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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 92253

108 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
April 28, 2023
Product types
Drug
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Central Admixture Pharmacy Services, Inc.

Dossier provenance

Source snapshots represented here

  • openFDA Drug Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

108 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

drug · product 1 of 108

Microplegia (MSA/MSG 0.92 Molar) packaged in 125 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0001-1.

D-0648-2023
Recall number
D-0648-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
307 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-894942, Exp 05/01/2023; 37-896485, Exp 05/07/2023; 37-896793, Exp 05/08/2023; 37-898247, Exp 05/14/2023; 37-899149, Exp 05/19/2023; 37-900610, Exp 05/25/2023

Distribution pattern

Nationwide in the USA.

drug · product 2 of 108

Cardioplegia Solution, Warm Induction 4:1 High Potassium (40 mEq) packaged in 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0002-1.

D-0649-2023
Recall number
D-0649-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
215 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-893802, Exp 04/28/2023; 37-894943, Exp 05/01/2023; 37-896487, Exp 05/07/2023; 37-898248, Exp 05/14/2023; 37-899171, Exp 05/19/2023

Distribution pattern

Nationwide in the USA.

drug · product 3 of 108

Cardioplegia Solution, Reperfusate No Potassium, packaged in 238.75 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0005-1.

D-0650-2023
Recall number
D-0650-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
255 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-893790, Exp 04/28/2023; 37-896488, Exp 05/07/2023; 37-898250, Exp 05/14/2023; 37-899235, Exp 05/19/2023; 37-900609, Exp 05/25/2023

Distribution pattern

Nationwide in the USA.

drug · product 4 of 108

Cardioplegia Solution, Reperfusate No Potassium, packaged in 477.5 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0006-1.

D-0651-2023
Recall number
D-0651-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
151 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-895691, Exp 05/05/2023; 37-896792, Exp 05/08/2023; 37-899170, Exp 05/19/2023

Distribution pattern

Nationwide in the USA.

drug · product 5 of 108

Cardioplegia Solution, Reperfusate 4:1 low potassium, 7.5 mEq K, packaged in 238.75 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0007-1.

D-0652-2023
Recall number
D-0652-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
140 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-896489, Exp 05/07/2023; 37-897805, Exp 05/12/2023; 37-900959, Exp 05/26/2023

Distribution pattern

Nationwide in the USA.

drug · product 6 of 108

Cardioplegia Solution, Reperfusate 4:1 low potassium, 15 mEq K, packaged in 477.5 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0008-1.

D-0653-2023
Recall number
D-0653-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
338 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-893847, Exp 04/28/2023; 37-895646, Exp 05/05/2023; 37-897804, Exp 05/12/2023; 37-899236, Exp 05/19/2023

Distribution pattern

Nationwide in the USA.

drug · product 7 of 108

Cardioplegia Solution, Reperfusate 4:1 low potassium/low tromethamine, 15 mEq K, packaged in 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0009-1.

D-0654-2023
Recall number
D-0654-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
254 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-893848, Exp 04/28/2023; 37-895681, Exp 05/05/2023; 37-899250, Exp 05/19/2023; 37-901355, Exp 05/27/2023

Distribution pattern

Nationwide in the USA.

drug · product 8 of 108

Cardioplegia Solution, Warm Induction 4:1 HIGH POTASSIUM/low tromethamine, 40 mEq K, packaged in 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0011-1.

D-0655-2023
Recall number
D-0655-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
12 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-897075, Exp 05/11/2023

Distribution pattern

Nationwide in the USA.

drug · product 9 of 108

Microplegia Solution, MSA/MSG 0.92 Molar with CP2D, packaged in 120 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0012-2.

D-0656-2023
Recall number
D-0656-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
144 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-893787, Exp 04/28/2023; 37-895645, Exp 05/05/2023; 37-897071, Exp 05/11/2023; 37-897802, Exp 05/12/2023; 37-899136, Exp 05/19/2023

Distribution pattern

Nationwide in the USA.

drug · product 10 of 108

Transplant Solution (Plasma-Lyte A), packaged in 165 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0014-2.

D-0657-2023
Recall number
D-0657-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
24 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-897801, Exp 05/12/2023

Distribution pattern

Nationwide in the USA.

drug · product 11 of 108

Cardioplegia Solution, Induction 4:1, High Potassium, 60 mEq K, packaged in 830 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0100-1.

D-0658-2023
Recall number
D-0658-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
267 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-894304, Exp 04/29/2023; 37-894946, Exp 05/01/2023; 37-896482, Exp 05/07/2023; 37-897933, Exp 05/13/2023; 37-900461, Exp 05/22/2023

Distribution pattern

Nationwide in the USA.

drug · product 12 of 108

Cardioplegia Solution, Induction 4:1, HIGH POTASSIUM/low tromethamine, 36 mEq K, packaged in 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-0101-1.

D-0659-2023
Recall number
D-0659-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
350 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-895647, Exp 05/05/2023; 37-898310, Exp 05/14/2023; 37-899622, Exp 05/20/2023; 37-900951, Exp 05/26/2023

Distribution pattern

Nationwide in the USA.

drug · product 13 of 108

Cardioplegia Solution, Induction 8:1 High Potassium, 108 mEq K, packaged in 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0102-1.

D-0660-2023
Recall number
D-0660-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
544 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-894305, Exp 04/29/2023; 37-896153, Exp 05/06/2023; 37-897073, Exp 05/11/2023; 37-897925, 37-897941, Exp 05/13/2023; 37-899607, 37-899608, Exp 05/20/2023; 37-900320, Exp 05/22/2023

Distribution pattern

Nationwide in the USA.

drug · product 14 of 108

Cardioplegia Solution, Maintenance 4:1 low potassium, 20 mEq K, packaged in 810 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0103-1.

D-0661-2023
Recall number
D-0661-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
269 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-893803, Exp 04/28/2023; 37-896483, Exp 05/07/2023; 37-897939, Exp 05/13/2023; 37-900952, Exp 05/26/2023

Distribution pattern

Nationwide in the USA.

drug · product 15 of 108

Cardioplegia Solution, Maintenance 4:1 low potassium/low tromethamine, 36 mEq K, packaged in 1000 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0104-1.

D-0662-2023
Recall number
D-0662-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
476 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-893850, Exp 04/28/2023; 37-894947, Exp 05/01/2023; 37-895695, Exp 05/05/2023; 37-896484, Exp 05/07/2023; 37-898314, Exp 05/14/2023; 37-898811, Exp 05/18/2023; 37-900616, Exp 05/25/2023

Distribution pattern

Nationwide in the USA.

drug · product 16 of 108

Cardioplegia Solution, Maintenance 8:1 low potassium, 24 mEq K, packaged in 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0105-1.

D-0663-2023
Recall number
D-0663-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
308 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-893846, Exp 04/28/2023; 37-895704, Exp 05/05/2023; 37-897079, Exp 05/11/2023; 37-897927, Exp 05/13/2023; 37-898814, Exp 05/18/2023; 37-900617, Exp 05/25/2023

Distribution pattern

Nationwide in the USA.

drug · product 17 of 108

Cardioplegia Solution, Induction 4:1 High Potassium, 30 mEq K, packaged in 415 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0106-1.

D-0664-2023
Recall number
D-0664-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
84 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-894307, Exp 04/29/2023; 37-896158, Exp 05/06/2023; 37-898281, Exp 05/14/2023; 37-900321, Exp 05/22/2023

Distribution pattern

Nationwide in the USA.

drug · product 18 of 108

Cardioplegia Solution, Induction 8:1 High Potassium/low dextrose, 100 mEq K, packaged in 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0107-1.

D-0665-2023
Recall number
D-0665-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
48 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-897926, Exp 05/13/2023; 37-900464, Exp 05/22/2023

Distribution pattern

Nationwide in the USA.

drug · product 19 of 108

Cardioplegia Solution, Induction 4:1 Plasma-Lyte/Tromethamine, High Potassium, packaged in 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0111-1.

D-0666-2023
Recall number
D-0666-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
613 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-894299, Exp 04/29/2023; 37-897051, Exp 05/11/2023; 37-897368, Exp 05/12/2023; 37-898794, Exp 05/18/2023; 37-899614, Exp 05/20/2023; 37-900608, Exp 05/25/2023

Distribution pattern

Nationwide in the USA.

drug · product 20 of 108

Cardioplegia Solution, Maintenance 4:1 Plasma-Lyte/Tromethamine, low potassium, packaged in 1000 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0112-1.

D-0667-2023
Recall number
D-0667-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
476 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-894300, Exp 04/29/2023; 37-896114, Exp 05/06/2023; 37-896417, Exp 05/07/2023; 37-897388, Exp 05/12/2023; 37-898798, Exp 05/18/2023; 37-899618, Exp 05/20/2023

Distribution pattern

Nationwide in the USA.

drug · product 21 of 108

Cardioplegia Solution, del Nido Formula, packaged in 1,052.8 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0202-1.

D-0668-2023
Recall number
D-0668-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
12,888 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-890033, 37-890035, Exp 04/28/2023; 37-890518, 37-890527, 37-890536, 37-890538, Exp 04/29/2023; 37-890844, 37-890845, Exp 04/30/2023; 37-891159, 37-891161, 37-891187, 37-891190, 37-891212, 37-891213, 37-891222, 37-891223, Exp 05/01/2023; 37-891432, 37-891433, 37-891434, 37-891435, 37-891440, 37-891442, 37-891445, 37-891446, 37-891447, Exp 05/02/2023; 37-891746, 37-891754, 37-891755, Exp 05/05/2023; 37-892005, 37-892007, Exp 05/06/2023; 37-892502, 37-892503, 37-892505, 37-892517, 37-892518, 37-892519, 37-892538, Exp 05/07/2023; 37-892871, 37-892873, 37-892874, 37-892879, 37-892880, 37-892886, 37-892887, 37-892888, 37-892899, Exp 05/08/2023; 37-893129, 37-893131, 37-893158, 37-893160, 37-893162, 37-893163, 37-893164, Exp 05/09/2023; 37-893681, 37-893689, 37-893698, 37-893760, 37-893761, 37-893762, Exp 05/13/2023; 37-894275, 37-894276, 37-894277, 37-894301, Exp 05/14/2023; 37-894651, 37-894654, 37-894658, 37-894660, 37-894662, 37-894663, Exp 05/15/2023; 37-894948, 37-894967, 37-894970, Exp 05/16/2023; 37-895276, 37-895278, 37-895281, 37-895284, 37-895285, 37-895286, 37-895289, 37-895297, Exp 05/19/2023; 37-895650, 37-895652, Exp 05/20/2023; 37-896051, 37-896052, 37-896054, 37-896055, 37-896057, 37-896058, 37-896455, Exp 05/21/2023; 37-896418, 37-896419, 37-896420, 37-896438, 37-896453, 37-896454, 37-896855, Exp 05/22/2023; 37-896814, 37-896816, 37-896818, 37-896823, 37-896824, 37-896841, 37-896843, 37-896942, Exp 05/23/2023; 37-897417, 37-897429, Exp 05/27/2023; 37-897856, 37-897857, 37-897858, 37-897880, 37-897881, 37-897882, 37-898264, Exp 05/28/2023; 37-898180, 37-898222, 37-898225, 37-898226, 37-898227, 37-898228, Exp 05/29/2023; 37-898487, 37-898488, 37-898490, Exp 05/30/2023; 37-898781, 37-898782, 37-898784, 37-898787, 37-898788, Exp 06/02/2023; 37-899102, 37-899103, 37-899104, 37-899105, Exp 06/03/2023; 37-899590, 37-899598, 37-899599, 37-900116, Exp 06/04/2023; 3700000900051, 37-900052, 37-900054, 37-900055, Exp 06/05/2023; 37-900306, 37-900309, 37-900310, 37-900311, 37-900313, 37-900314, 37-900315, 37-900316, Exp 06/06/2023

Distribution pattern

Nationwide in the USA.

drug · product 22 of 108

Cardioplegia Solution, Modified St Thomas Solution, low potassium, HIGH SODIUM BICARBONATE, 62 mEq K, packaged in 1000 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0203-1.

D-0669-2023
Recall number
D-0669-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
182 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-894704, Exp 04/30/2023; 37-896126, Exp 05/06/2023; 37-898276, Exp 05/14/2023; 37-899141, Exp 05/19/2023

Distribution pattern

Nationwide in the USA.

drug · product 23 of 108

Cardioplegia Solution, Modified St Thomas Solution, HIGH POTASSIUM, HIGH SODIUM BICARBONATE, 106 mEq K, packaged in 1000 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0204-1.

D-0670-2023
Recall number
D-0670-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
241 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-894705, Exp 04/30/2023; 37-896127, Exp 05/06/2023; 37-898278, Exp 05/14/2023; 37-899148, Exp 05/19/2023; 37-900619, Exp 05/25/2023

Distribution pattern

Nationwide in the USA.

drug · product 24 of 108

Cardioplegia Solution, Maintenance 4:1 in Ringer's, low potassium, 12 mEq K, packaged in 504.8 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0205-1.

D-0671-2023
Recall number
D-0671-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
280 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-894325, Exp 04/29/2023; 37-895211, Exp 05/04/2023; 37-899265, Exp 05/19/2023

Distribution pattern

Nationwide in the USA.

drug · product 25 of 108

Cardioplegia Solution, Induction 4:1 in Ringer's, HIGH POTASSIUM, 48 mEq K, packaged in 522.8 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0206-1.

D-0672-2023
Recall number
D-0672-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
333 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-894326, Exp 04/29/2023; 37-895212, Exp 05/04/2023; 37-896794, Exp 05/08/2023; 37-897286, Exp 05/12/2023; 37-899267, Exp 05/19/2023

Distribution pattern

Nationwide in the USA.

drug · product 26 of 108

Cardioplegia Solution, Modified St Thomas Formula, HIGH POTASSIUM, 122 mEq K, packaged in 1000 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0209-1.

D-0673-2023
Recall number
D-0673-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
329 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-893789, Exp 04/28/2023; 37-894318, Exp 04/29/2023; 37-895648, Exp 05/05/2023; 37-897301, Exp 05/12/2023; 37-898815, Exp 05/18/2023

Distribution pattern

Nationwide in the USA.

drug · product 27 of 108

Cardioplegia Solution, Modified St Thomas Formula, low potassium, 70 mEq K, packaged in 1000 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0210-1.

D-0674-2023
Recall number
D-0674-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
208 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-894320, Exp 04/29/2023; 37-894324, Exp 04/29/2023; 37-897297, Exp 05/12/2023; 37-898509, Exp 05/15/2023

Distribution pattern

Nationwide in the USA.

drug · product 28 of 108

Cardioplegia Solution, Maintenance 4:1 Plasmalyte, low potassium, low K, packaged in 1047 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0211-1.

D-0675-2023
Recall number
D-0675-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
226 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-894309, 37-894321, Exp 04/29/2023; 37-896159, Exp 05/06/2023; 37-898510, Exp 05/15/2023; 37-900324, Exp 05/22/2023

Distribution pattern

Nationwide in the USA.

drug · product 29 of 108

Cardioplegia Solution, Induction 4:1 Plasmalyte, HIGH POTASSIUM, HIGH K, packaged in 542 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0212-1.

D-0676-2023
Recall number
D-0676-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
52 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-895217, Exp 05/04/2023; 37-898803, Exp 05/18/2023; 37-900614, Exp 05/25/2023

Distribution pattern

Nationwide in the USA.

drug · product 30 of 108

Microplegia Solution, HIGH POTASSIUM (100 mEq), packaged in 200 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0213-1.

D-0677-2023
Recall number
D-0677-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
79 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-895226, Exp 05/04/2023; 37-900615, Exp 05/25/2023

Distribution pattern

Nationwide in the USA.

drug · product 31 of 108

Cardioplegia Solution, Induction 8:1 non-enriched, HIGH POTASSIUM, 70 mEq K, packaged in 300 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0214-1.

D-0678-2023
Recall number
D-0678-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
363 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-894310, Exp 04/29/2023; 37-895259, Exp 05/04/2023; 37-898303, Exp 05/14/2023; 37-901367, Exp 05/27/2023

Distribution pattern

Nationwide in the USA.

drug · product 32 of 108

Cardioplegia Solution, Maintenance 8:1 non-enriched, low potassium, 24 mEq K, packaged in 300 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0215-1.

D-0679-2023
Recall number
D-0679-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
325 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-895694, 37-896050, Exp 05/05/2023; 37-898304, Exp 05/14/2023; 37-899234, Exp 05/19/2023; 37-901375, Exp 05/27/2023

Distribution pattern

Nationwide in the USA.

drug · product 33 of 108

Cardioplegia Solution, LEESBURG CARDIOPLEGIA, packaged in 1030.2 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0218-1.

D-0680-2023
Recall number
D-0680-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
79 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-895256, Exp 05/04/2023; 37-898816, Exp 05/18/2023

Distribution pattern

Nationwide in the USA.

drug · product 34 of 108

Modified del Nido Microplegia, packaged in 40 mL per syringe, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0219-1.

D-0681-2023
Recall number
D-0681-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
690 syringes

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-893821, Exp 04/28/2023; 37-894813, 37-894815, Exp 04/30/2023; 37-895489, 37-895490, Exp 05/05/2023; 37-897810, 37-897811, Exp 05/13/2023; 37-899585, Exp 05/20/2023

Distribution pattern

Nationwide in the USA.

drug · product 35 of 108

Neonatal TPN Starter Bag, Amino Acids (Trophamine) 2%/Dextrose 10%, packaged in 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0400-1.

D-0682-2023
Recall number
D-0682-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
80 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-895214, Exp 05/04/2023; 37-897950, Exp 05/13/2023; 37-899603, Exp 05/20/2023

Distribution pattern

Nationwide in the USA.

drug · product 36 of 108

Neonatal TPN Starter Bag, Amino Acids (Trophamine) 3%/Dextrose 10% with CALCIUM, packaged in 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0405-1.

D-0683-2023
Recall number
D-0683-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
558 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-893806, Exp 04/28/2023; 37-894701, Exp 04/30/2023; 37-895626, Exp 05/05/2023; 37-897277, Exp 05/12/2023; 37-899175, Exp 05/19/2023; 37-900971, Exp 05/26/2023

Distribution pattern

Nationwide in the USA.

drug · product 37 of 108

Neonatal TPN Starter Bag, Amino Acids (Trophamine) 3.5%/Dextrose 10%, packaged in 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0406-1.

D-0684-2023
Recall number
D-0684-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
71 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-894328, Exp 04/29/2023; 37-897792, Exp 05/12/2023

Distribution pattern

Nationwide in the USA.

drug · product 38 of 108

Neonatal TPN Starter Bag, Amino Acids (Trophamine) 3.5%/Dextrose 10% with CALCIUM, packaged in 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0407-1.

D-0685-2023
Recall number
D-0685-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
138 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-894709, Exp 04/30/2023; 37-896128, Exp 05/06/2023; 37-897894, Exp 05/13/2023

Distribution pattern

Nationwide in the USA.

drug · product 39 of 108

Neonatal TPN Starter Bag, Amino Acids (Trophamine) 4%/Dextrose 10%, packaged in 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0408-1.

D-0686-2023
Recall number
D-0686-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
167 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-896130, Exp 05/06/2023; 37-897957, Exp 05/13/2023; 37-899605, Exp 05/20/2023; 37-901357, Exp 05/27/2023

Distribution pattern

Nationwide in the USA.

drug · product 40 of 108

Neonatal TPN Starter Bag, Amino Acids (Trophamine) 3%/Dextrose 5% with CALCIUM, packaged in 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0413-1.

D-0687-2023
Recall number
D-0687-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
258 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-894313, Exp 04/29/2023; 37-895257, Exp 05/04/2023; 37-897360, Exp 05/12/2023; 37-897890, Exp 05/13/2023; 37-900964, Exp 05/26/2023

Distribution pattern

Nationwide in the USA.

drug · product 41 of 108

Neonatal TPN Starter Bag, Amino Acids (Trophamine) 2%/Dextrose 10% with CALCIUM and HEPARIN, packaged in 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0416-1.

D-0688-2023
Recall number
D-0688-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
139 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-897800, Exp 05/12/2023; 37-897895, Exp 05/13/2023

Distribution pattern

Nationwide in the USA.

drug · product 42 of 108

Neonatal TPN Starter Bag, Amino Acids (Trophamine) 2.5%/Dextrose 10% with CALCIUM and HEPARIN, packaged in 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0418-1.

D-0689-2023
Recall number
D-0689-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
92 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-894334, Exp 04/29/2023; 37-898299, Exp 05/14/2023

Distribution pattern

Nationwide in the USA.

drug · product 43 of 108

Neonatal TPN Starter Bag, Amino Acids (Trophamine) 3%/Dextrose 5% with CALCIUM and HEPARIN, packaged in 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0419-1.

D-0690-2023
Recall number
D-0690-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
418 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-893810, Exp 04/28/2023; 37-894698, Exp 04/30/2023; 37-896144, Exp 05/06/2023; 37-897896, Exp 05/13/2023; 37-899172, Exp 05/19/2023

Distribution pattern

Nationwide in the USA.

drug · product 44 of 108

Neonatal TPN Starter Bag, Amino Acids (Trophamine) 3%/Dextrose 10% with CALCIUM and HEPARIN, packaged in 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0420-1.

D-0691-2023
Recall number
D-0691-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
877 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-894314, Exp 04/29/2023; 37-894690, 37-894699, Exp 04/30/2023; 37-895627, Exp 05/05/2023; 37-896494, Exp 05/07/2023; 37-897082, Exp 05/11/2023; 37-897955, Exp 05/13/2023; 37-899254, Exp 05/19/2023; 37-900057, 37-900060, Exp 05/21/2023

Distribution pattern

Nationwide in the USA.

drug · product 45 of 108

Neonatal TPN Starter Bag, Amino Acids (Trophamine) 3.5%/Dextrose 10% with CALCIUM and HEPARIN, packaged in 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0421-1.

D-0692-2023
Recall number
D-0692-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
427 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-893804, Exp 04/28/2023; 37-894713, Exp 04/30/2023; 37-896134, Exp 05/06/2023; 37-896497, Exp 05/07/2023; 37-897310, Exp 05/12/2023; 37-899623, Exp 05/20/2023

Distribution pattern

Nationwide in the USA.

drug · product 46 of 108

Neonatal TPN Starter Bag, Amino Acids (Trophamine) 4%/Dextrose 10% with CALCIUM and HEPARIN, packaged in 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0422-1.

D-0693-2023
Recall number
D-0693-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
747 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-893819, Exp 04/28/2023; 37-894702, 37-894710, Exp 04/30/2023; 37-895215, Exp 05/04/2023; 37-897282, Exp 05/12/2023; 37-897921, Exp 05/13/2023; 37-898309, Exp 05/14/2023; 37-899199, Exp 05/19/2023; 37-900058, Exp 05/21/2023

Distribution pattern

Nationwide in the USA.

drug · product 47 of 108

Neonatal TPN Starter Bag, Amino Acids (Trophamine) 6%/Dextrose 10% with CALCIUM and HEPARIN, packaged in 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0423-1.

D-0694-2023
Recall number
D-0694-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
128 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-896152, Exp 05/06/2023; 37-897923, Exp 05/13/2023; 37-899173, Exp 05/19/2023

Distribution pattern

Nationwide in the USA.

drug · product 48 of 108

Neonatal TPN Starter Bag, Amino Acids (Trophamine) 2%/Dextrose 10% with low calcium and HEPARIN, packaged in 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0425-1.

D-0695-2023
Recall number
D-0695-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
135 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-894712, Exp 04/30/2023; 37-897924, Exp 05/13/2023; 37-899606, Exp 05/20/2023

Distribution pattern

Nationwide in the USA.

drug · product 49 of 108

Neonatal TPN Starter Bag, Amino Acids (Trophamine) 3%/Dextrose 5% with low calcium and HEPARIN, packaged in 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0427-1.

D-0696-2023
Recall number
D-0696-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
259 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-894338, Exp 04/29/2023; 37-896505, Exp 05/07/2023; 37-898301, Exp 05/14/2023; 37-898305, Exp 05/14/2023; 37-900061, Exp 05/21/2023

Distribution pattern

Nationwide in the USA.

drug · product 50 of 108

Neonatal TPN Starter Bag, Amino Acids (Trophamine) 3%/Dextrose 10% with low calcium and HEPARIN, packaged in 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0428-1.

D-0697-2023
Recall number
D-0697-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
485 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-893805, Exp 04/28/2023; 37-894711, Exp 04/30/2023; 37-895258, Exp 05/04/2023; 37-896501, Exp 05/07/2023; 37-898160, Exp 05/13/2023; 37-900064, Exp 05/21/2023; 37-900620, Exp 05/25/2023

Distribution pattern

Nationwide in the USA.

drug · product 51 of 108

Neonatal PN Starter Bag, Amino Acids (Trophamine) 3.5%/Dextrose 10% with low calcium and HEPARIN, packaged in 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100 Allentown, PA 18106, NDC 71285-0429-1.

D-0698-2023
Recall number
D-0698-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
328 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-894695, Exp 04/30/2023; 37-895693, Exp 05/05/2023; 37-900065, Exp 05/21/2023; 37-900622, Exp 05/25/2023

Distribution pattern

Nationwide in the USA.

drug · product 52 of 108

Neonatal TPN Starter Bag, Amino Acids (Trophamine) 6%/Dextrose 10% with low calcium and HEPARIN, packaged in 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0430-1.

D-0699-2023
Recall number
D-0699-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
60 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-896506, Exp 05/07/2023; 37-898306, Exp 05/14/2023; 37-900062, Exp 05/21/2023

Distribution pattern

Nationwide in the USA.

drug · product 53 of 108

Neonatal TPN Starter Bag, Amino Acids (Trophamine) 4.5%/Dextrose 10% with HEPARIN, packaged in 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0432-1.

D-0700-2023
Recall number
D-0700-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
175 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-894962, Exp 05/01/2023; 37-898285, Exp 05/14/2023

Distribution pattern

Nationwide in the USA.

drug · product 54 of 108

EPINEPHrine added to dextrose 5%, 2 mg/250 mL* (8 mcg/mL), 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6030-1.

D-0701-2023
Recall number
D-0701-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
3338 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-884448, Exp 05/04/2023; 37-887386, Exp 05/16/2023; 37-888271, Exp 05/21/2023; 37-891189, Exp 05/31/2023; 37-893456, Exp 06/11/2023; 37-894656, Exp 06/14/2023; 37-898333, Exp 06/28/2023; 37-898559, Exp 06/29/2023

Distribution pattern

Nationwide in the USA.

drug · product 55 of 108

oxyTOCIN 20 units added to dextrose 5%/Lactated Ringer's 1,000 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6031-1.

D-0702-2023
Recall number
D-0702-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
7595 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-883206, 37-883207, 37-883210, 37-883213, 37-883216, 37-883217, 37-883217, Exp 04/30/2023; 37-884447, 37-884450, Exp 05/04/2023; 37-886269, Exp 05/11/2023; 37-887516, Exp 05/16/2023; 37-888306, 37-888308, 37-888310, 37-888311, Exp 05/21/2023; 37-890097, 37-890099, 37-890101, 37-890108, Exp 05/28/2023; 37-892636, 37-892637, 37-892639, 37-892640, Exp 06/06/2023; 37-894451, 37-894452, 37-894476, 37-894482, Exp 06/13/2023; 37-895311, 37-895312, 37-895313, Exp 06/18/2023; 37-895804, Exp 06/19/2023; 37-896607, Exp 06/21/2023

Distribution pattern

Nationwide in the USA.

drug · product 56 of 108

oxyTOCIN 30 units added to dextrose 5%/Lactated Ringer's 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6032-1.

D-0703-2023
Recall number
D-0703-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
2624 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-883948, Exp 05/02/2023; 37-886037, 37-886040, Exp 05/10/2023; 37-889593, Exp 05/24/2023; 37-891270, Exp 05/31/2023; 37-893223, Exp 06/08/2023; 37-896230, Exp 06/20/2023; 37-898520, Exp 06/29/2023

Distribution pattern

Nationwide in the USA.

drug · product 57 of 108

oxyTOCIN 10 units added to Lactated Ringer's 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 72185-6036-1.

D-0704-2023
Recall number
D-0704-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
2989 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-891283, Exp 05/06/2023; 37-892501, Exp 05/12/2023; 37-894413, Exp 05/19/2023; 37-896228, Exp 05/26/2023; 37-896815, 37-896820, 37-896826, Exp 05/28/2023; 37-900126, Exp 06/10/2023

Distribution pattern

Nationwide in the USA.

drug · product 58 of 108

oxyTOCIN 15 units added to Lactated Ringer's 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6037-1.

D-0705-2023
Recall number
D-0705-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
560 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-891282, Exp 05/06/2023; 37-900124, Exp 06/10/2023

Distribution pattern

Nationwide in the USA.

drug · product 59 of 108

oxyTOCIN 20 units added to Lactated Ringer's 1,000 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6038-1.

D-0706-2023
Recall number
D-0706-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
14362 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-889158, 37-889187, 37-889189, Exp 04/28/2023; 37-889494, 37-889507, 37-889522, 37-889525, 37-889527, 37-889608, Exp 04/29/2023; 37-889906, 37-889912, 37-889913, Exp 04/30/2023; 37-890110, 37-890121, Exp 05/03/2023; 37-891160, 37-891162, 37-891186, 37-891188, 37-891199, 37-891211, Exp 05/06/2023; 37-891564, 37-891565, 37-891567, 37-891569, 37-891570, Exp 05/07/2023; 37-892591, Exp 05/12/2023; 37-892893, 37-892897, 37-892900, 37-892902, 37-892903, 37-892904, 37-892909, 37-892910, Exp 05/13/2023; 37-894715, 37-894720, 37-894749, 37-894754, 37-894762, 37-894763, 37-894765, Exp 05/20/2023; 37-894991, 37-894992, 37-894993, Exp 05/21/2023; 37-896187, 37-896188, 37-896190, 37-896191, 37-896199, 05/26/2023; 37-896521, 37-896522, 37-896523, Exp 05/27/2023; 37-896883, 37-896884, Exp 05/28/2023; 37-900067, 37-900068, Exp 06/10/2023

Distribution pattern

Nationwide in the USA.

drug · product 60 of 108

oxyTOCIN 30 units added to Lactated Ringer's 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6039-1.

D-0707-2023
Recall number
D-0707-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
21871 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-889853, 37-889854, 37-889856, Exp 04/30/2023; 37-890087, 37-890088, 37-890095, 37-890098, 37-890100, 37-890107, 37-890109, Exp 05/03/2023; 37-890876, 37-890878, 37-890885, 37-890891, Exp 05/05/2023; 37-891572, Exp 05/07/2023; 37-892504, 37-892510, 37-892512, 37-892520, 37-892560, 37-892575, 37-892585, 37-892587, Exp 05/12/2023; 37-892988, 37-892989, Exp 05/13/2023; 37-894323, 37-894356, 37-894366, 37-894385, 37-894386, 37-894402, 37-894409, 37-894410, Exp 05/19/2023; 37-894778, Exp 05/20/2023; 37-894998, 37-894999, 37-895000, 37-895001, 37-895002, Exp 05/21/2023; 37-896186, 37-896189, 37-896192, 37-896194, 37-896200, 37-896202, 37-896227, 37-896231, 37-896240, 37-896241, Exp 05/26/2023; 37-896844, 37-896851, 37-896853, 37-896856, Exp 05/28/2023; 37-897827, 37-897836, 37-897837, 37-897853, 37-897854, 37-897928, Exp 06/02/2023; 37-900117, 37-900122, 37-900123, Exp 06/10/2023

Distribution pattern

Nationwide in the USA.

drug · product 61 of 108

oxyTOCIN 15 units added to 0.9% sodium chloride 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 72185-6042-1.

D-0708-2023
Recall number
D-0708-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
3865 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-883926, Exp 05/02/2023; 37-886032, Exp 05/10/2023; 37-887681, Exp 05/17/2023; 37-888317, Exp 05/21/2023; 37-890906, Exp 05/30/2023; 37-892146, Exp 06/05/2023; 37-892507, Exp 06/06/2023; 37-894483, Exp 06/13/2023; 37-896595, Exp 06/21/2023; 37-898568, Exp 06/29/2023

Distribution pattern

Nationwide in the USA.

drug · product 62 of 108

oxyTOCIN 20 units added to 0.9% sodium chloride 1,000 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 72185-6043-1.

D-0709-2023
Recall number
D-0709-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
5544 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-883938, Exp 05/02/2023; 37-884910, 37-884915, Exp 05/07/2023; 37-886041, Exp 05/10/2023; 37-887515, 37-887520, Exp 05/16/2023; 37-888318, Exp 05/21/2023; 37-888847, Exp 05/22/2023; 37-890535, Exp 05/29/2023; 37-890957, Exp 05/30/2023; 37-891566, 37-891568, Exp 06/01/2023; 37-892156, Exp 06/05/2023; 37-893165, 37-893166, Exp 06/08/2023; 37-893994, 37-893995, Exp 06/12/2023; 37-895771, 37-895773, 37-895775, Exp 06/19/2023; 37-896614, Exp 06/21/2023; 37-900377, Exp 07/06/2023

Distribution pattern

Nationwide in the USA.

drug · product 63 of 108

oxyTOCIN 30 units added to 0.9% sodium chloride 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6044-1.

D-0710-2023
Recall number
D-0710-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
104807 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-883041, 37-883043, 37-883044, 37-883045, 37-883047, 37-883059, 37-883060, 37-883067, 37-883071, 37-883072, 37-883131, 37-883185, Exp 04/28/2023; 37-883492, 37-883499, 37-883501, 37-883503, 37-883514, 37-883525, 37-883526, 37-883539, 37-883540, 37-883548, 37-883549, 37-883550, 37-883551, Exp 05/01/2023; 37-884229, 37-884230, 37-884245, 37-884249, 37-884252, 37-884256, 37-884260, 37-884261, 37-884262, 37-884266, 37-884270, Exp 05/03/2023; 37-884452, 37-884453, 37-884457, 37-884461, 37-884464, 37-884466, 37-884468, 37-884470, 37-884472, 37-884473, Exp 05/04/2023; 37-884793, 37-884812, 37-884817, 37-884821, 37-884822, 37-884830, 37-884833, 37-884874, 37-884881, 37-884886, 37-884895, 37-884905, 37-884907, 37-884916, 37-884917, Exp 05/05/2023; 37-884807, 37-884941, 37-884942, 37-884943, 37-884944, 37-884945, 37-884946, 37-884954, 37-884955, 37-884956, Exp 05/07/2023; 37-885187, 37-885217, 37-885244, 37-885247, 37-885261, 37-885268, 37-885279, 37-885282, 37-885291, 37-885293, Exp 05/08/2023; 37-885584, 37-885598, 37-885608, Exp 05/09/2023; 37-886056, 37-886057, 37-886060, 37-886081, 37-886082, 37-886088, 37-886089, Exp 05/10/2023; 37-886251, 37-886256, 37-886257, 37-886259, 37-886263, 37-886264, Exp 05/11/2023; 37-886499, 37-886503, 37-886510, 37-886527, 37-886530, 37-886532, 37-886534, 37-886538, 37-886541, 37-886542, 37-886543, Exp 05/14/2023; 37-887304, 37-887306, 37-887307, 37-887308, 37-887309, 37-887310, 37-887311, 37-887312, Exp 05/16/2023; 37-887672, 37-887693, 37-887718, 37-887724, 37-887728, 37-887753, Exp 05/17/2023; 37-888081, 37-888082, 37-888084, 37-888086, Exp 05/18/2023; 37-888304, 37-888305, 37-888307, 37-888309, 37-888312, 37-888313, 37-888315, 37-888316, Exp 05/21/2023; 37-888695, 37-888705, 37-888722, 37-888742, 37-888764, Exp 05/22/2023; 37-889048, 37-889049, 37-889061, 37-889065, 37-889118, 37-889133, 37-889139, Exp 05/23/2023; 37-889530, 37-889534, 37-889541, 37-889561, 37-889562, 37-889563, 37-889571, 37-889573, 37-889703, Exp 05/24/2023; 37-889733, 37-889747, 37-889793, 37-889803, 37-889828, 37-889829, 37-889839, 37-889841, 37-889847, 37-889851, Exp 05/25/2023; 37-890413, 37-890419, 37-890427, 37-890430, 37-890435, 37-890443, 37-890444, 37-890473, Exp 05/29/2023; 37-890958, Exp 05/30/2023; 37-891217, 37-891221, 37-891224, 37-891229, 37-891231, 37-891233, 37-891248, Exp 05/31/2023; 37-891475, 37-891479, 37-891481, 37-891484, 37-891486, 37-891488, 37-891531, 37-891549, 37-891550, 37-891562, Exp 06/01/2023; 37-892164, 37-892183, 37-892195, Exp 06/05/2023; 37-892878, 37-892883, 37-892885, 37-892891, 37-892892, 37-892895, 37-892896, Exp 06/07/2023; 37-893167, 37-893168, 37-893200, 37-893203, 37-893205, 37-893206, 37-893219, Exp 06/08/2023; 37-893457, 37-893462, 37-893468, Exp 06/11/2023; 37-893798, 37-893799, 37-893808, 37-893809, 37-893814, 37-893844, Exp 06/12/2023; 37-894655, 37-894661, 37-894664, 37-894666, 37-894686, 37-894703, Exp 06/14/2023; 37-895029, 37-895030, 37-895036, 37-895037, 37-895038, 37-895048, 37-895056, 37-895063, 37-895068, 37-895072, 37-895073, 37-895074, 37-895075, Exp 06/15/2023; 37-895260, 37-895271, 37-895273, 37-895274, Exp 06/18/2023; 37-895623, 37-895624, 37-895644, 37-895653, 37-895661, 37-895676, 37-895677, 37-895678, 37-895679, 37-895774, 37-895776, Exp 06/19/2023; 37-896536, 37-896540, 37-896541, 37-896542, 37-896543, 37-896547, 37-896566, 37-896585, 37-896587, 37-896596, 37-896597, 37-896598, 37-896599, 37-896615, Exp 06/21/2023; 37-896864, 37-896868, 37-896870, 37-896877, 37-896879, 37-896882, 37-896882, 37-896885, 37-896899, 37-896901, 37-896903, 37-896914, 37-896915, 37-896916, Exp 06/22/2023; 37-897454, 37-897500, Exp 06/26/2023; 37-898273, Exp 06/28/2023; 37-898517, Exp 06/29/2023

Distribution pattern

Nationwide in the USA.

drug · product 64 of 108

oxyTOCIN 60 units added to 0.9% sodium chloride 1,000 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6045-1.

D-0711-2023
Recall number
D-0711-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
1332 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-883073, Exp 04/28/2023; 37-887776, Exp 05/17/2023; 37-889209, Exp 05/23/2023; 37-892588, Exp 06/06/2023; 37-894449, Exp 06/13/2023; 37-898552, Exp 06/29/2023

Distribution pattern

Nationwide in the USA.

drug · product 65 of 108

dilTIAZem added to dextrose 5%, 125 mg/125 mL* (1 mg/mL), 125 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 72185-6054-1.

D-0712-2023
Recall number
D-0712-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
1230 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-896365, 37-896367, 37-896370, Exp 05/31/2023; 37-896857, 37-896858, 37-896859, Exp 06/02/2023

Distribution pattern

Nationwide in the USA.

drug · product 66 of 108

dilTIAZem added to 0.9% sodium chloride, 125 mg/125 mL* (1 mg/mL), 125 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6055-1.

D-0713-2023
Recall number
D-0713-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
3040 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-896374, 37-896375, Exp 05/31/2023; 37-896876, 37-896878, Exp 06/02/2023; 37-897077, 37-897078, Exp 06/05/2023; 37-900074, 37-900075, 37-900076, 37-900111, 37-900112, 37-900115, Exp 06/15/2023; 37-900328, Exp 06/16/2023

Distribution pattern

Nationwide in the USA.

drug · product 67 of 108

norepinephrine 4 mg added to dextrose 5% 250 mL*, 16 mcg/mL, 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6056-1.

D-0714-2023
Recall number
D-0714-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
2041 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-884760, Exp 05/05/2023; 37-885601, Exp 05/09/2023; 37-887668, Exp 05/17/2023; 37-889594, Exp 05/24/2023; 37-892622, Exp 06/06/2023; 37-894316, Exp 06/13/2023

Distribution pattern

Nationwide in the USA.

drug · product 68 of 108

PHENYLephrine added to 0.9% sodium chloride, 10 mg/250 mL* (40 mcg/mL), 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6058-1.

D-0715-2023
Recall number
D-0715-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
6407 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-884272, Exp 05/03/2023; 37-887513, Exp 05/16/2023; 37-888083, Exp 05/18/2023; 37-889123, 37-889423, Exp 05/23/2023; 37-891563, Exp 06/01/2023; 37-892577, 37-892582, Exp 06/06/2023; 37-893248, 37-893257, Exp 06/08/2023; 37-894436, Exp 06/13/2023; 37-895805, Exp 06/19/2023; 37-898324, Exp 06/28/2023

Distribution pattern

Nationwide in the USA.

drug · product 69 of 108

potassium phosphate 15 mmole added to 0.9% sodium chloride 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6060-1.

D-0716-2023
Recall number
D-0716-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
9432 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-883769, Exp 05/02/2023; 37-884449, Exp 05/04/2023; 37-885585, Exp 05/09/2023; 37-885922, Exp 05/10/2023; 37-886526, Exp 05/14/2023; 37-887387, Exp 05/16/2023; 37-887659, 37-887662, Exp 05/17/2023; 37-889064, Exp 05/23/2023; 37-889735, 37-889745, Exp 05/25/2023; 37-890036, 37-890055, Exp 05/28/2023; 37-890934, Exp 05/30/2023; 37-892890, Exp 06/07/2023; 37-893813, Exp 06/12/2023; 37-894317, Exp 06/13/2023; 37-895275, Exp 06/18/2023; 37-896822, 37-896852, Exp 06/22/2023; 37-897826, 37-897839, Exp 06/27/2023

Distribution pattern

Nationwide in the USA.

drug · product 70 of 108

vancomycin added to 0.9% sodium chloride, 1 g/250 mL* (4 mg/mL), 25 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6064-1.

D-0717-2023
Recall number
D-0717-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
4390 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-885351, Exp 05/08/2023; 37-885979, Exp 05/10/2023; 37-887721, Exp 05/17/2023; 37-889212, Exp 05/23/2023; 37-889607, Exp 05/24/2023; 37-891247, Exp 05/31/2023; 37-892937, Exp 06/07/2023; 37-894025, Exp 06/12/2023; 37-894748, Exp 06/14/2023; 37-895282, Exp 06/18/2023; 37-896173, Exp 06/20/2023

Distribution pattern

Nationwide in the USA.

drug · product 71 of 108

vancomycin added to 0.9% sodium chloride, 750 mg/250 mL* (3 mg/mL), 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6071-1.

D-0718-2023
Recall number
D-0718-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
3075 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-884161, Exp 05/03/2023; 37-885995, 37-885997, Exp 05/10/2023; 37-887729, Exp 05/17/2023; 37-889595, Exp 05/24/2023; 37-891272, Exp 05/31/2023; 37-892162, Exp 06/05/2023; 37-894716, Exp 06/14/2023

Distribution pattern

Nationwide in the USA.

drug · product 72 of 108

vancomycin added to dextrose 5%, 1.25 g/250 mL* (5 mg/mL), 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6073-1.

D-0719-2023
Recall number
D-0719-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
13772 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-883198, 37-883202, 37-883203, 37-883204, Exp 04/30/2023; 37-883799, Exp 05/02/2023; 37-884159, Exp 05/03/2023; 37-884888, 37-884892, 37-884899, 37-884901, Exp 05/07/2023; 37-886836, 37-886855, 37-886861, Exp 05/15/2023; 37-887381, Exp 05/16/2023; 37-887664, Exp 05/17/2023; 37-888256, 37-888259, 37-888267, Exp 05/21/2023; 37-888624, 37-888625, Exp 05/22/2023; 37-890038, 37-890041, 37-890042, Exp 05/28/2023; 37-890331, 37-890336, 37-890350, Exp 05/29/2023; 37-891163, Exp 05/31/2023; 37-892008, 37-892012, 37-892015, Exp 06/05/2023; 37-892882, 37-892884, Exp 06/07/2023

Distribution pattern

Nationwide in the USA.

drug · product 73 of 108

vancomycin added to 0.9% sodium chloride, 1.25 g/250 mL* (5 mg/mL), 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6074-1.

D-0720-2023
Recall number
D-0720-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
27780 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-883407, 37-883436, Exp 05/01/2023; 37-883796, 37-883797, 37-883800, 37-883802, 37-883806, Exp 05/02/2023; 37-884162, 37-884163, Exp 05/03/2023; 37-885332, 37-885336, 37-885337, Exp 05/08/2023; 37-885749, 37-885753, 37-885755, Exp 05/09/2023; 37-886008, 37-886027, 37-886031, 37-886035, Exp 05/10/2023; 37-886273, 37-886274, 37-886275, Exp 05/11/2023; 37-887448, 37-887457, Exp 05/16/2023; 37-887765, 37-887772, 37-887775, Exp 05/17/2023; 37-888062, 37-888072, Exp 05/18/2023; 37-888811, 37-888817, Exp 05/22/2023; 37-889193, 37-889208, 37-889210, Exp 05/23/2023; 37-889450, 37-889451, 37-889454, Exp 05/24/2023; 37-890940, 37-890941, 37-890952, Exp 05/30/2023; 37-891137, 37-891138, 37-891139, Exp 05/31/2023; 37-892633, 37-892634, 37-892635, Exp 06/06/2023; 37-892934, 37-892961, 37-892964, 37-892965, Exp 06/07/2023; 37-893524, Exp 06/11/2023; 37-893993, 37-893996, Exp 06/12/2023; 37-894465, 37-894466, 37-894467, 37-894468, Exp 06/13/2023; 37-894706, 37-894714, Exp 06/14/2023; 37-895680, 37-895682, Exp 06/19/2023; 37-896123, Exp 06/20/2023; 37-896564, 37-896579, 37-896586, Exp 06/21/2023

Distribution pattern

Nationwide in the USA.

drug · product 74 of 108

vancomycin added to dextrose 5%, 1.5 g/250 mL* (6 mg/mL), 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6075-1.

D-0721-2023
Recall number
D-0721-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
10282 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-883196, 37-883197, 37-883205, Exp 04/30/2023; 37-884882, 37-884890, 37-884898, Exp 05/07/2023; 37-886840, 37-886858, 37-886863, Exp 05/15/2023; 37-887365, Exp 05/16/2023; 37-887663, Exp 05/17/2023; 37-888254, 37-888257, 37-888265, 37-888303, Exp 05/21/2023; 37-889453, Exp 05/24/2023; 37-890037, 37-890039, 37-890043, Exp 05/28/2023; 37-890330, 37-890333, 37-890344, Exp 05/29/2023; 37-892009, 37-892011, 37-892016, Exp 06/05/2023; 37-892881, Exp 06/07/2023; 37-893448, Exp 06/11/2023; 37-895221, Exp 06/18/2023; 37-898530, Exp 06/29/2023

Distribution pattern

Nationwide in the USA.

drug · product 75 of 108

vancomycin added to 0.9% sodium chloride, 1.5 g/250 mL* (6 mg/mL), 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6076-1.

D-0722-2023
Recall number
D-0722-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
9037 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-883390, 37-883435, Exp 05/01/2023; 37-884157, Exp 05/03/2023; 37-885716, 37-886036, 37-886039, Exp 05/09/2023; 37-887499, 37-887500, Exp 05/16/2023; 37-887778, Exp 05/17/2023; 37-888105, Exp 05/18/2023; 37-889216, Exp 05/23/2023; 37-890923, 37-890928, 37-890936, Exp 05/30/2023; 37-891271, Exp 05/31/2023; 37-892649, Exp 06/06/2023; 37-892962, Exp 06/07/2023; 37-893966, 37-893967, 37-893969, 37-893998, Exp 06/12/2023; 37-896160, 37-896162, 37-896171, Exp 06/20/2023

Distribution pattern

Nationwide in the USA.

drug · product 76 of 108

vancomycin added to 0.9% sodium chloride, 2 g/500 mL* (4 mg/mL), 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6078-1.

D-0723-2023
Recall number
D-0723-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
7632 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-884151, 37-884153, Exp 05/03/2023; 37-885670, 37-885869, 37-885900, Exp 05/09/2023; 37-886271, Exp 05/11/2023; 37-886857, 37-886862, 37-886865, 37-886923, Exp 05/15/2023; 37-889190, 37-889191, Exp 05/23/2023; 37-889596, Exp 05/24/2023; 37-890482, 37-890487, 37-890488, Exp 05/29/2023; 37-891230, Exp 05/31/2023; 37-892589, 37-892590, Exp 06/06/2023; 37-893779, 37-893780, 37-893781, Exp 06/12/2023; 37-894665, 37-894667, Exp 06/14/2023; 37-895608, 37-895625, Exp 06/19/2023; 37-896519, Exp 06/21/2023

Distribution pattern

Nationwide in the USA.

drug · product 77 of 108

PHENYLephrine added to 0.9% sodium chloride, 40 mg/250 mL* (160 mcg/mL), 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6092-1.

D-0724-2023
Recall number
D-0724-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
14205 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-883910, Exp 05/02/2023; 37-884221, Exp 05/03/2023; 37-884756, Exp 05/05/2023; 37-885358, Exp 05/08/2023; 37-885683, Exp 05/09/2023; 37-886267, 37-886268, Exp 05/11/2023; 37-886539, Exp 05/14/2023; 37-887458, 37-887459, Exp 05/16/2023; 37-888080, Exp 05/18/2023; 37-889192, Exp 05/23/2023; 37-889575, 37-889578, Exp 05/24/2023; 37-889852, 37-889855, Exp 05/25/2023; 37-890120, 37-890126, Exp 05/28/2023; 37-891485, 37-891491, Exp 06/01/2023; 37-892901, 37-892966, Exp 06/07/2023; 37-893236, 37-893237, Exp 06/08/2023; 37-893997, Exp 06/12/2023; 37-894777, Exp 06/14/2023; 37-895317, 37-895321, 37-895323, Exp 06/18/2023; 37-896201, Exp 06/20/2023; 37-896923, Exp 06/22/2023; 37-898558, Exp 06/29/2023

Distribution pattern

Nationwide in the USA.

drug · product 78 of 108

vancomycin added to 0.9% sodium chloride, 1.5 g/500 mL* (3 mg/mL), 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6176-1.

D-0725-2023
Recall number
D-0725-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
11338 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-883372, 37-883387, Exp 05/01/2023; 37-883790, Exp 05/02/2023; 37-884160, Exp 05/03/2023; 37-885320, 37-885321, 37-885324, Exp 05/08/2023; 37-885921, 37-885928, 37-885930, Exp 05/10/2023; 37-886270, Exp 05/11/2023; 37-887511, Exp 05/16/2023; 37-887666, 37-887670, Exp 05/17/2023; 37-888115, Exp 05/18/2023; 37-888841, Exp 05/22/2023; 37-889457, 37-889462, Exp 05/24/2023; 37-892638, 37-892641, 37-892648, Exp 06/06/2023; 37-892907, Exp 06/07/2023; 37-894437, 37-894443, 37-894450, Exp 06/13/2023; 37-895707, 37-895718, 37-895723, Exp 06/19/2023; 37-896532, 37-896535, Exp 06/21/2023; 37-898527, Exp 06/29/2023

Distribution pattern

Nationwide in the USA.

drug · product 79 of 108

heparin added to 0.9% sodium chloride, 7,500 units/1,000 mL* (7.5 units/mL), 1000 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-7009-1.

D-0726-2023
Recall number
D-0726-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
3055 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-888668, 37-888685, 37-888701, Exp 05/02/2023; 37-890550, 37-890556, Exp 05/09/2023; 37-892201, 37-892216, Exp 05/16/2023; 37-893866, 37-893917, 37-893918, Exp 05/23/2023; 37-895705, 37-895717, Exp 05/30/2023

Distribution pattern

Nationwide in the USA.

drug · product 80 of 108

PHENYLephrine added to 0.9% sodium chloride, 25 mg/250 mL* (100 mcg/mL), 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-7011-1.

D-0727-2023
Recall number
D-0727-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
5304 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-883924, Exp 05/02/2023; 37-884918, Exp 05/07/2023; 37-885677, Exp 05/09/2023; 37-887318, Exp 05/16/2023; 37-889211, Exp 05/23/2023; 37-889848, Exp 05/25/2023; 37-891150, Exp 05/31/2023; 37-892482, Exp 06/06/2023; 37-894484, Exp 06/13/2023; 37-896458, 37-896480, Exp 06/21/2023; 37-897967, Exp 06/27/2023; 37-898551, Exp 06/29/2023

Distribution pattern

Nationwide in the USA.

drug · product 81 of 108

potassium phosphate 30 mmole added to 0.9% sodium chloride 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-7016-1.

D-0728-2023
Recall number
D-0728-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
2146 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-883219, Exp 04/30/2023; 37-885926, Exp 05/10/2023; 37-887382, Exp 05/16/2023; 37-889455, Exp 05/24/2023; 37-890060, Exp 05/28/2023; 37-893444, Exp 06/11/2023; 37-894987, Exp 06/15/2023

Distribution pattern

Nationwide in the USA.

drug · product 82 of 108

EPINEPHrine added to dextrose 5%, 4 mg/250 mL* (16 mcg/mL), 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-7018-1.

D-0729-2023
Recall number
D-0729-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
5627 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-883218, Exp 04/30/2023; 37-885235, Exp 05/08/2023; 37-885923, Exp 05/10/2023; 37-889050, Exp 05/23/2023; 37-890053, 37-890054, Exp 05/28/2023; 37-891439, 37-891441, Exp 06/01/2023; 37-892500, Exp 06/06/2023; 37-894308, Exp 06/13/2023; 37-896125, Exp 06/20/2023; 37-896926, Exp 06/22/2023; 37-900396, Exp 07/06/2023

Distribution pattern

Nationwide in the USA.

drug · product 83 of 108

EPINEPHrine added to dextrose 5%, 8 mg/250 mL* (32 mcg/mL), 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-7019-1.

D-0730-2023
Recall number
D-0730-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
2542 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-884156, Exp 05/03/2023; 37-885207, Exp 05/08/2023; 37-885929, Exp 05/10/2023; 37-886496, Exp 05/14/2023; 37-886817, Exp 05/15/2023; 37-887420, Exp 05/16/2023; 37-893786, Exp 06/12/2023; 37-894303, Exp 06/13/2023; 37-897893, Exp 06/27/2023; 37-900073, Exp 07/05/2023

Distribution pattern

Nationwide in the USA.

drug · product 84 of 108

heparin added to 0.9% sodium chloride, 4,000 units/1,000 mL* (4 units/mL), 1,000 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-7022-1.

D-0731-2023
Recall number
D-0731-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
11117 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-888633, 37-888637, 37-888641, 37-888658, 37-888666, 37-888839, Exp 05/02/2023; 37-890332, 37-890383, 37-890394, 37-890424, 37-890428, 37-890442, Exp 05/09/2023; 37-892010, 37-892021, 37-892046, 37-892061, 37-892116, 37-892120, 37-892150, 37-892153, Exp 05/16/2023; 37-893467, 37-893469, 37-893470, 37-893471, 37-893508, 37-893512, 37-893519, Exp 05/22/2023; 37-893925, 37-893937, 37-893939, 37-893940, 37-893958, 37-893968, Exp 05/23/2023; 37-895218, 37-895220, 37-895224, 37-895231, 37-895236, 37-895305, 37-895306, Exp 05/29/2023; 37-895754, 37-895756, 37-895757, Exp 05/30/2023

Distribution pattern

Nationwide in the USA.

drug · product 85 of 108

heparin added to 0.9% sodium chloride, 5,000 units/500 mL* (10 units/mL), 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-7023-1.

D-0732-2023
Recall number
D-0732-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
5207 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-888736, 37-888769, Exp 05/02/2023; 37-890465, 37-890483, Exp 05/09/2023; 37-892088, 37-892117, 37-892119, 37-892145, Exp 05/16/2023; 37-893759, 37-893765, Exp 05/23/2023; 37-895742, 37-895751, Exp 05/30/2023

Distribution pattern

Nationwide in the USA.

drug · product 86 of 108

PHENYLephrine added to 0.9% sodium chloride, 20 mg/250 mL* (80 mcg/mL), 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-7025-1.

D-0733-2023
Recall number
D-0733-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
13953 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-883074, Exp 04/28/2023; 37-883237, 37-883238, Exp 04/30/2023; 37-883940, Exp 05/02/2023; 37-884271, Exp 05/03/2023; 37-884749, 37-884751, Exp 05/05/2023; 37-885338, Exp 05/08/2023; 37-885756, Exp 05/09/2023; 37-886272, Exp 05/11/2023; 37-887512, Exp 05/16/2023; 37-888027, 37-888030, 37-888040, 37-888052, 37-888063, Exp 05/18/2023; 37-888314, Exp 05/21/2023; 37-890489, 37-890497, 37-890534, Exp 05/29/2023; 37-890933, Exp 05/30/2023; 37-891152, Exp 05/31/2023; 37-892985, 37-892986, 37-892995, Exp 06/07/2023; 37-893511, 37-893517, Exp 06/11/2023; 37-896481, Exp 06/21/2023; 37-897828, Exp 06/27/2023; 37-898523, Exp 06/29/2023

Distribution pattern

Nationwide in the USA.

drug · product 87 of 108

NORepinephrine added to 0.9% sodium chloride, 16 mg/250 mL* (64 mcg/mL), 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-7036-1.

D-0734-2023
Recall number
D-0734-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
6341 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-882998, 37-883005, 37-883145, Exp 04/28/2023; 37-883144, 37-883220, 37-883221, 37-883222, Exp 04/30/2023; 37-883925, Exp 05/02/2023; 37-884180, 37-884181, Exp 05/03/2023; 37-884505, 37-884506, 37-884507, 37-884508, 37-884509, Exp 05/04/2023; 37-884834, 37-884869, 37-884870, Exp 05/07/2023; 37-886058, Exp 05/10/2023; 37-886536, 37-886537, Exp 05/14/2023; 37-887062, 37-887389, Exp 05/15/2023; 37-887784, 37-887787, Exp 05/17/2023; 37-888029, 37-888048, Exp 05/18/2023; 37-888261, 37-888263, 37-888269, 37-888282, 37-888292, 37-888294, 37-888301, 37-888302, Exp 05/21/2023; 37-890058, 37-890064, 37-890074, 37-890076, Exp 05/28/2023; 37-891747, 37-891748, 37-891750, 37-891751, 37-891753, Exp 06/04/2023; 37-893530, 37-893531, 37-893532, Exp 06/11/2023; 37-894760, 37-894761, Exp 06/14/2023; 37-894988, 37-894990, Exp 06/15/2023; 37-896260, Exp 06/20/2023; 37-896621, Exp 06/21/2023; 37-898518, 37-898519, Exp 06/29/2023; 37-898789, 37-898790, 37-898791, 37-898792, 37-898793, Exp 07/02/2023; 37-899718, Exp 07/04/2023; 37-900591, 37-900596, Exp 07/09/2023; 37-901149, Exp 07/10/2023

Distribution pattern

Nationwide in the USA.

drug · product 88 of 108

phenylephrine 50 mg added to 0.9% sodium chloride 250 mL*, 200 mcg/mL*, 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-7039-1.

D-0735-2023
Recall number
D-0735-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
1735 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-887056, 37-887057, 37-887059, Exp 05/15/2023; 37-893807, Exp 06/12/2023; 37-896880, Exp 06/22/2023

Distribution pattern

Nationwide in the USA.

drug · product 89 of 108

vancomycin added to 0.9% sodium chloride, 1.75 g/500 mL* (3.5 mg/mL), 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-7060-1.

D-0736-2023
Recall number
D-0736-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
8252 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-884152, 37-884158, Exp 05/03/2023; 37-885300, 37-885302, 37-885307, Exp 05/08/2023; 37-887418, 37-887431, 37-887432, Exp 05/16/2023; 37-888850, 37-888852, 37-888853, Exp 05/22/2023; 37-889188, Exp 05/23/2023; 37-890892, 37-890894, 37-890897, Exp 05/30/2023; 37-891232, Exp 05/31/2023; 37-892014, 37-892017, Exp 06/05/2023; 37-894411, 37-894412, 37-894414, Exp 06/13/2023; 37-894659, Exp 06/14/2023; 37-896078, 37-896089, 37-896097, Exp 06/20/2023; 37-897369, Exp 06/26/2023

Distribution pattern

Nationwide in the USA.

drug · product 90 of 108

diphenhydrAMINE 25 mg added to 0.9% sodium chloride 50 mL in 100 mL Partial Additive Bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-7089-1.

D-0737-2023
Recall number
D-0737-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
5627 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-884145, 37-884154, Exp 05/03/2023; 37-885931, Exp 05/10/2023; 37-888293, Exp 05/21/2023; 37-889057, 37-889063, Exp 05/23/2023; 37-891437, Exp 06/01/2023; 37-893455, Exp 06/11/2023; 37-893788, Exp 06/12/2023; 37-894302, Exp 06/13/2023; 37-894652, Exp 06/14/2023; 37-896817, Exp 06/22/2023; 37-897263, Exp 06/26/2023

Distribution pattern

Nationwide in the USA.

drug · product 91 of 108

diphenhydrAMINE 50 mg added to 0.9% sodium chloride 50 mL in 100 mL Partial Additive Bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-7090-1.

D-0738-2023
Recall number
D-0738-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
3999 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-884155, Exp 05/03/2023; 37-885992, Exp 05/10/2023; 37-887348, Exp 05/16/2023; 37-887660, Exp 05/17/2023; 37-889052, Exp 05/23/2023; 37-891155, 37-891156, Exp 05/31/2023; 37-891443, Exp 06/01/2023; 37-892475, Exp 06/06/2023

Distribution pattern

Nationwide in the USA.

drug · product 92 of 108

heparin added to 0.9% sodium chloride, 2,500 units/250 mL* (10 units/mL), 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-8000-1.

D-0739-2023
Recall number
D-0739-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
1300 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-888810, Exp 05/02/2023; 37-892217, Exp 05/16/2023; 37-895759, Exp 05/30/2023; 37-899174, Exp 06/13/2023

Distribution pattern

Nationwide in the USA.

drug · product 93 of 108

oxyTOCIN 40 units added to 0.9% sodium chloride 1,000 bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-8069-1.

D-0740-2023
Recall number
D-0740-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
2186 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-886265, Exp 05/11/2023; 37-886266, Exp 05/11/2023; 37-889903, Exp 05/25/2023; 37-890551, Exp 05/29/2023; 37-892521, 37-892620, Exp 06/06/2023; 37-896246, 37-896247, Exp 06/20/2023; 37-898553, Exp 06/29/2023

Distribution pattern

Nationwide in the USA.

drug · product 94 of 108

tromethamine 0.3 Molar, 50 mL syringe, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-8086-2.

D-0741-2023
Recall number
D-0741-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
225 syringes

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-884580, Exp 05/04/2023; 37-887061, Exp 05/15/2023; 37-892981, Exp 06/07/2023

Distribution pattern

Nationwide in the USA.

drug · product 95 of 108

EPINEPHrine added to 0.9% sodium chloride, 4 mg/250 mL* (16 mcg/mL), 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-8093-1.

D-0742-2023
Recall number
D-0742-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
8171 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-882988, Exp 04/28/2023; 37-883194, 37-883208, Exp 04/30/2023; 37-884746, Exp 05/05/2023; 37-885215, Exp 05/08/2023; 37-885927, Exp 05/10/2023; 37-887044, 37-887051, Exp 05/15/2023; 37-887667, Exp 05/17/2023; 37-888297, 37-888298, Exp 05/21/2023; 37-890886, Exp 05/30/2023; 37-891438, Exp 06/01/2023; 37-892497, Exp 06/06/2023; 37-893159, Exp 06/08/2023; 37-893843, Exp 06/12/2023; 37-894649, Exp 06/14/2023; 37-896928, Exp 06/22/2023; 37-899304, Exp 07/03/2023

Distribution pattern

Nationwide in the USA.

drug · product 96 of 108

NORepinephrine added to dextrose 5%, 16 mg/250 mL* (64 mcg/mL), 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-8095-1.

D-0743-2023
Recall number
D-0743-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
2890 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-883007, 37-883015, 37-883017, Exp 04/28/2023; 37-883236, Exp 04/30/2023; 37-884187, 37-884189, 37-884190, Exp 05/03/2023; 37-884567, 37-884568, 37-884569, Exp 05/04/2023; 37-887789, 37-887790, Exp 05/17/2023; 37-889142, 37-889143, 37-889144, 37-889149, Exp 05/23/2023; 37-889606, Exp 05/24/2023; 37-890519, 37-890528, Exp 05/29/2023; 37-890946, 37-890951, Exp 05/30/2023; 37-891281, 37-891284, 37-891292, 37-891294, Exp 05/31/2023; 37-891756, 37-891757, Exp 06/04/2023; 37-897959, 37-897961, Exp 06/27/2023; 37-898795, Exp 07/02/2023

Distribution pattern

Nationwide in the USA.

drug · product 97 of 108

NORepinephrine added to 0.9% sodium chloride, 8 mg/250 mL* (32 mcg/mL), 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-8096-1.

D-0744-2023
Recall number
D-0744-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
6414 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-882989, Exp 04/28/2023; 37-883827, 37-883829, 37-883830, 37-883833, 37-883858, Exp 05/02/2023; 37-884758, Exp 05/05/2023; 37-885357, Exp 05/08/2023; 37-885748, 37-885751, Exp 05/09/2023; 37-887409, 37-887410, Exp 05/16/2023; 37-888863, 37-888867, Exp 05/22/2023; 37-889226, Exp 05/23/2023; 37-889576, 37-889577, Exp 05/24/2023; 37-889804, 37-889817, 37-889830, Exp 05/25/2023; 37-891280, Exp 05/31/2023; 37-891758, 37-891759, Exp 06/04/2023; 37-894311, 37-894315, 37-894319, Exp 06/13/2023; 37-895304, Exp 06/18/2023; 37-896544, 37-896545, 37-896546, 37-896552, Exp 06/21/2023; 37-898514, 37-898515, 37-898516, Exp 06/29/2023; 37-899305, Exp 07/03/2023; 37-900362, Exp 07/06/2023

Distribution pattern

Nationwide in the USA.

drug · product 98 of 108

NORepinephrine added to 0.9% sodium chloride, 4 mg/250 mL* (16 mcg/mL), 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-8097-1.

D-0745-2023
Recall number
D-0745-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
4994 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-884510, Exp 05/04/2023; 37-885671, Exp 05/09/2023; 37-886285, Exp 05/11/2023; 37-888322, Exp 05/21/2023; 37-888851, Exp 05/22/2023; 37-889840, Exp 05/25/2023; 37-890130, Exp 05/28/2023; 37-890966, Exp 05/30/2023; 37-893529, Exp 06/11/2023; 37-894766, Exp 06/14/2023; 37-895300, 37-895301, Exp 06/18/2023; 37-898521, Exp 06/29/2023; 37-900338, Exp 07/06/2023

Distribution pattern

Nationwide in the USA.

drug · product 99 of 108

heparin added to 0.9% sodium chloride, 2,500 units/500 mL* (5 units/mL), 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-8100-1.

D-0746-2023
Recall number
D-0746-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
2992 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-888833, Exp 05/02/2023; 37-890537, Exp 05/09/2023; 37-892161, 37-892163, Exp 05/16/2023; 37-893979, 37-893992, Exp 05/23/2023; 37-895755, 37-895758, Exp 05/30/2023

Distribution pattern

Nationwide in the USA.

drug · product 100 of 108

vasopressin 20 units added to 0.9% sodium chloride 100 mL*, 0.2 units/mL*, 100 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-9000-1.

D-0747-2023
Recall number
D-0747-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
1858 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-886252, 37-886254, Exp 05/11/2023; 37-889741, 37-889746, Exp 05/25/2023; 37-891444, Exp 06/01/2023; 37-893155, 37-893156, Exp 06/08/2023; 37-896812, Exp 06/22/2023

Distribution pattern

Nationwide in the USA.

drug · product 101 of 108

vasopressin 40 units added to 0.9% sodium chloride 100 mL*, 0.4 units/mL*, 100 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-9001-1.

D-0748-2023
Recall number
D-0748-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
100 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-889738, 37-889742, Exp 05/25/2023

Distribution pattern

Nationwide in the USA.

drug · product 102 of 108

vasopressin 50 units added to 0.9% sodium chloride 50 mL*, 1 unit/mL*, 50 mL in 100 mL Partial Additive Bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-9002-1.

D-0749-2023
Recall number
D-0749-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
4259 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-883209, 37-883211, 37-883212, 37-883214, 37-883215, Exp 04/30/2023; 37-883776, Exp 05/02/2023; 37-884451, Exp 05/04/2023; 37-884805, 37-884806, 37-884808, 37-884810, 37-884811, Exp 05/07/2023; 37-886498, 37-886506, 37-886507, 37-886509, 37-886511, 37-886512, Exp 05/14/2023; 37-887319, 37-887321, Exp 05/16/2023; 37-889572, 37-889574, Exp 05/24/2023; 37-890881, 37-890883, 37-890884, 37-890887, Exp 05/30/2023; 37-892003, 37-892004, 37-892006, Exp 06/05/2023; 37-893157, Exp 06/08/2023; 37-893460, 37-893461, 37-893463, Exp 06/11/2023; 37-894619, 37-894648, 37-894650, Exp 06/14/2023; 37-895213, 37-895216, 37-895219, 37-895223, 37-895225, Exp 06/18/2023; 37-896813, Exp 06/22/2023; 37-897069, 37-897074, Exp 06/25/2023

Distribution pattern

Nationwide in the USA.

drug · product 103 of 108

MSA 7.84% MSG 8.56% (0.92M) Comp. Sol. 1000 ml bag, Rx only, Central Admixture Pharmacy Services, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-8029-1, code 7128580291.

D-0750-2023
Recall number
D-0750-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
653 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-882955, Exp 04/29/2023; 37-884753, 37-884755, Exp 05/06/2023; 37-887536, 37-887537, Exp 05/17/2023; 37-888532, Exp 05/23/2023; 37-892474, Exp 06/07/2023; 37-896761, Exp 06/23/2023; 37-897261, Exp 06/27/2023

Distribution pattern

Nationwide in the USA.

drug · product 104 of 108

Sodium Phosphates Injection 4 mEq/3 mMol/mL, 500 ml bag, Rx only, Central Admixture Pharmacy Services, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-8077-1, code 7128580771.

D-0751-2023
Recall number
D-0751-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
3165 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-883239, 37-883240, Exp 05/01/2023; 37-884419, 37-884423, Exp 05/04/2023; 37-889009, Exp 05/23/2023; 37-890261, 37-890262, Exp 05/29/2023; 37-891250, Exp 05/31/2023; 37-891412, Exp 06/01/2023; 37-895488, Exp 06/19/2023; 37-896456, Exp 06/21/2023; 37-898159, Exp 06/28/2023

Distribution pattern

Nationwide in the USA.

drug · product 105 of 108

Potassium Acetate Injection, 2 mEq/mL, 500 ml bag, Rx only, Central Admixture Pharmacy Services, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-8078-1, code 7128580781.

D-0752-2023
Recall number
D-0752-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
3326 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-884108, 37-884109, Exp 05/03/2023; 37-884957, Exp 05/07/2023; 37-885047, 37-885048, Exp 05/08/2023; 37-885919, Exp 05/10/2023; 37-889426, 37-889432, Exp 05/24/2023; 37-891933, Exp 06/05/2023; 37-894274, Exp 06/13/2023; 37-896048, 37-896049, Exp 06/20/2023; 37-897798, Exp 06/27/2023

Distribution pattern

Nationwide in the USA.

drug · product 106 of 108

Lidocaine 2% HCl Inj, 500mL bag, Rx only, Central Admixture Pharmacy Services, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-8091-1, code 7128580911.

D-0753-2023
Recall number
D-0753-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
1516 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-870983, Exp 06/10/2023; 37-879653, 37-879654, Exp 07/16/2023; 37-883186, Exp 07/29/2023; 37-888533, Exp 08/20/2023; 37-893416, Exp 09/09/2023

Distribution pattern

Nationwide in the USA.

drug · product 107 of 108

HyperLyte CR Injection, 500 mL bag, Rx only, Central Admixture Pharmacy Services, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-8094-1, code 7128580941.

D-0754-2023
Recall number
D-0754-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
554 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-874236, Exp 06/20/2023; 37-878694, Exp 07/10/2023

Distribution pattern

Nationwide in the USA.

drug · product 108 of 108

HyperLyte CR Injection, 250 mL bag, Rx only, Central Admixture Pharmacy Services, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-8094-2, code 7128580942.

D-0755-2023
Recall number
D-0755-2023
Initiated
April 28, 2023
Classification
Class II
Status
Terminated
Quantity
1673 bags

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Code information

Lot # 37-885553, 37-885554, Exp 05/09/2023; 37-887923, 37-887924, Exp 05/18/2023; 37-890778, 37-890779, Exp 05/30/2023; 37-892847, Exp 06/07/2023; 37-895049, Exp 06/15/2023; 37-898480, 37-898481, Exp 06/29/2023

Distribution pattern

Nationwide in the USA.