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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 68532

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

Open FDA event record

Event summary

Timeline bucket
May 28, 2014
Product types
Drug
Classifications
Class I
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

4 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 4

PEDIATRIC CARDIOPLEGIA, 255 mL, Rx Only, Central Admixture Pharmacy Services, Inc., Livonia, MI 48150

D-1559-2014
Recall number
D-1559-2014
Initiated
May 28, 2014
Classification
Class I
Status
Terminated
Quantity
1 dose

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
microbial contamination

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Non Sterility; microbial contamination identified as Aspergillus species

Code information

Lot # 13-920741-0-1 EXP 21 JUN 2014

Distribution pattern

Michigan and Wisconsin

drug · product 2 of 4

del Nido Cardioplegia with Lidocaine 1052.8 ml, Rx Only, Central Admixture Pharmacy Services, Inc., Livonia, MI 48150

D-1560-2014
Recall number
D-1560-2014
Initiated
May 28, 2014
Classification
Class I
Status
Terminated
Quantity
31 doses

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
microbial contamination

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Non Sterility; microbial contamination identified as Aspergillus species

Code information

Lot# 13-920742-0-1 EXP 21 JUN 2014 and Lot# 13-920452-0-1 through 13-920452-0-30, EXP 21 JUN 2014

Distribution pattern

Michigan and Wisconsin

drug · product 3 of 4

adenosine 90 mg in 0.9% sodium chloride/90 mL, Rx Only, Central Admixture Pharmacy Services, Inc., Livonia, MI 48150

D-1561-2014
Recall number
D-1561-2014
Initiated
May 28, 2014
Classification
Class I
Status
Terminated
Quantity
5 doses

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
microbial contamination

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Non Sterility; microbial contamination identified as Aspergillus species

Code information

Lot# 13-920757-0-1 through Lot# 13-920757-0-5 (5 total doses) EXP 06 JUL 2014

Distribution pattern

Michigan and Wisconsin

drug · product 4 of 4

LOW Potassium Cardioplegia 792 mL, Rx Only, Central Admixture Pharmacy Services, Inc., Livonia, MI 48150

D-1562-2014
Recall number
D-1562-2014
Initiated
May 28, 2014
Classification
Class I
Status
Terminated
Quantity
4 doses

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
microbial contamination

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Non Sterility; microbial contamination identified as Aspergillus species

Code information

Lot # 13-920739-01 through Lot # 13-920739-04 (4 total doses) EXP 21 Jun 2014

Distribution pattern

Michigan and Wisconsin