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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 90336

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

Open FDA event record

Event summary

Timeline bucket
May 25, 2022
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Mckesson Medical-Surgical Inc. Corporate Office

Dossier provenance

Source snapshots represented here

  • openFDA Device 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.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

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

55 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.

device · product 1 of 55

a. Rapid Test Kit Coag-Sense Professional Blood Coagulation Test Prothrombin Time Test (PT/INR) Whole Blood Sample 50 Tests-IVD. Part No. 0356-50. b. Coagulation Control Kit Coag-Sense PT / INR Test (Prothrombin Time Test) Low Level / High Level 10 Strips Part No. 03P69-10.

Z-1583-2022
Recall number
Z-1583-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
a. 27 boxes b. 1 box

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

a. GTIN: 00861900000336; 10861900000395; 00861900000398. Lot codes distributed between 5/30/2021 - 8/24/2021. b. GTIN 00861900000343 Lots Distributed: 8/20/2021 - 8/20/2021

Distribution pattern

US Nationwide

device · product 2 of 55

Ethicon SURGIFLO Hemostatic Matrix Kit with Thrombin (6/CS) Ref: 2994 Mfg: FERROSAN MEDICAL DEVICES A/S Indicated in surgical procedures (other than ophthalmic) as an adjunct to hemostasis when control of bleeding by ligature or other conventional methods is ineffective or impractical.

Z-1584-2022
Recall number
Z-1584-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
2 cases

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: 15712123000288; 25712123000285 Lot 262801 Lots Distributed: 6/1/2021 - 6/2/2021

Distribution pattern

US Nationwide

device · product 3 of 55

HORIBA ABX MEDICAL INC ABX PENTRA ETCHING CP System Fluid ABX Pentra Eching Solution CP For ABX Pentra 400 Clinical Chemistry Analyzer 25 mL. Ref: 1220001769

Z-1585-2022
Recall number
Z-1585-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
3 each

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: 03610230005514 Lots Distributed:5/30/2021 - 6/9/2021

Distribution pattern

US Nationwide

device · product 4 of 55

a. ABX PENTRA CREATININE 120CP JAFFE 120/130. Ref: A11A01933. b. Reagent General Chemistry Creatinine Model Number: 1220001933

Z-1586-2022
Recall number
Z-1586-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
a. 28 b. 22

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: 03610230005736 Lots Distributed: 5/30/2021 - 9/8/2021

Distribution pattern

US Nationwide

device · product 5 of 55

a. McKesson Rapid Test Kit McKesson Consult Fertility Test hCG Pregnancy Test Serum / Urine Sample 25 Tests. Model Number: 5002. b. McKesson Consult Rapid Test Kit McKesson Consult Fertility Test hCG Pregnancy Test Urine Sample 25 Tests Model Number: 5000. c. McKesson Medical-Surgical McKesson TEST KIT, PREG HCG CASSETTE WAIVED Model Number: 5001

Z-1587-2022
Recall number
Z-1587-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
a. 108 b. 838 c. 1225

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: 10612479218625; 20612479202768 all lots and expiration dates received during July 4th through September 30th, 2021. b. GTIN: 10612479218618; 20612479202751 All lots received between 7/4/21-9/30/21. c. GTIN: 10612479218601; 20612479202744

Distribution pattern

US Nationwide

device · product 6 of 55

Alere Toxicology TABLET, INSTANT BLUING F/DRUGSCREEN Model Number: 7875

Z-1588-2022
Recall number
Z-1588-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
1 Btl

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: Unknown All lots received between 7/4/21-9/30/21

Distribution pattern

US Nationwide

device · product 7 of 55

Drugs of Abuse Tests: a. Wondfo Tdip Drugs of Abuse Test Tdip Single Drug Fentanyl (FEN) Urine Sample 25 Tests. Model Number: AWFTY-114. b. Alere Drugs of Abuse Test E-Z Split Key Cup 12-Drug Panel AMP, BAR, BUP, BZO, COC, mAMP/MET, MDMA, MOP, MTD, OXY, PPX, THC Urine Sample 25 Tests Model Number: DOA-1127-041-19. c. Instant Technologies, Inc. Drugs of Abuse Test iCup A.D. 5-Drug Panel with Adulterants AMP, COC, mAMP/MET, OPI, THC (OX, pH, SG) Urine Sample 25 Tests Model Number: I-DUA-157-013. d. Instant Technologies, Inc. Drugs of Abuse Test iCup A.D. 6-Drug Panel with Adulterants AMP, BZO, COC, mAMP/MET, OPI, THC, (OX, pH, SG) Urine Sample Tests Model Number: I-DUA-167-022. e. Alere Drugs of Abuse Test iCup Dx Pro 2 10-Drug Panel with Adulterants AMP, BAR, BUP, BZO, COC, mAMP/MET, OPI300, OXY, MTD, THC (CR, OX, SG) Urine Sample 25 Tests Model Number: I-DXP-2107-01. f. Alere Drugs of Abuse Test iScreen 5-Drug Panel AMP, COC, mAMP/MET, OPI, THC Urine Sample 25 Tests Model Number: IS5M. g. Instant Technologies, Inc. Drugs of Abuse Test T-Cube 7-Drug Panel AMP50, COC20, mAMP/MET50, OPI40, OXY20, PCP10, THC40 Saliva Sample 25 Tests Model Number: TCUBE-7PCPB. h. Wondfo Drugs of Abuse Test with Adulterants Tcup 14-Drug Panel AMP1000, BAR300, BZO300, BUP10, COC300, mAMP/MET1000, MDMA500, MTD300, MOP(OPI300), OXY100, PCP25, PPX300, TCA1000, THC50 (CR, pH, SG) Urine Sample 25 Tests Model Number: TDOA-1145A3. i. Instant Technologies, Inc. Drugs of Abuse Test UScreen 12-Drug Panel with Adulterants AMP, BAR, BZO, COC, mAMP/MET, MDMA, MOP, MTD, OXY, PCP, TCA, THC, (CR, pH, SG) Urine Sample 25 Tests Model Number: USSCUPA-12CLIA. j. Instant Technologies, Inc. Drugs of Abuse Test UScreen 12-Drug Panel with Adulterants AMP, BAR, BUP, BZO, COC, mAMP/MET, MDMA, MOP, MTD, OXY, PCP, THC (CR, pH, SG) Urine Sample 25 Tests Model Number: USSCupA-12BUP300. k. Alere Drugs of Abuse Test E-Z Split Key Cup 6-Drug Panel AMP, BZO, COC, mAMP/MET, OPI, THC Urine Sample 25 Tests Model Number: DOA-2167-019. l. Alere Drugs of Abuse Test E-Z Split Key Cup A.D. 5-Drug Panel with Adulterants AMP, COC, mAMP/MET, OPI, THC (CR, GL, NI, OX, pH, SG) Urine Sample 25 Tests Model Number: DUD-157-012-019. m. WONDFO USA CO., LTD. Wondfo Drug Test Dip Card Drugs of Abuse Test Tdip Single Drug Buprenorphine (BUP) Urine Sample 25 Tests Model Number: WDBU-114.

Z-1589-2022
Recall number
Z-1589-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
a. unk b. 6 c. 1 d. 1 e. 67 f. 1 g. 10 h. 51 i. 27 j. 105 k. 4 l. 2 m. 3

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

a. GTIN: Unknown All lots received between 7/4/21-9/30/21. b. GTIN:00815845020782; 10815845020789 All lots received between 7/4/21-9/30/21. c. GTIN:00858945006072; 10858945006079 All lots received between 7/4/21-9/30/21. d. GTIN: 00858945006133; 10858945006130 All lots received between 7/4/21-9/30/21. e. GTIN: 00817405020355; 00858945006829 All lots received between 7/4/21-9/30/21. f. GTIN: 00858945006508; 10858945006505 All lots received between 7/4/21-9/30/21. g. GTIN: 00817405020959 All lots received between 7/4/21-9/30/21. h. GTIN: 00816862020076; 10816862020073; 00816862029079; 00816862025071 All lots received between 7/4/21-9/30/21. i. GTIN: 00817405021192 All lots received between 7/4/21-9/30/21. j. GTIN: 00858998006104 All lots received between 7/4/21-9/30/21. k. GTIN: 00815845020720; 10815845020727 All lots received between 7/4/21-9/30/21. l. GTIN: 00815845020355; 10815845020352. m. GTIN: 00816862025415.

Distribution pattern

US Nationwide

device · product 8 of 55

a. Alcon Clear Care Contact Lens Solution Clear Care 12 oz. Solution, Model Number: 65035820, Model Number: USSCupA-12BUP300. b. Alcon Contact Lens Solution Opti Free Replenish 4 oz. Solution Model Number: 00065035604 Model Number: USSCupA-12BUP300. c. Alcon Contact Lens Solution Opti Free Replenish 10 oz. Solution Model Number: 00065035610. d. Alcon Contact Lens Solution Opti Free Replenish 2 oz. Solution Model Number: 00065135658.

Z-1590-2022
Recall number
Z-1590-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
a. 3 b. 91 c. 45 d. 2

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

a. GTIN: 00047113609126 EA; 20300650358204 CS. All lots received between 7/4/21-9/30/21. b. GTIN: 00300650356350 EA; 20300650356354 CS All lots received between 7/4/21-9/30/21. c. GTIN: 00300650356107 EA; 20300650357207 CS All lots received between 7/4/21-9/30/21. d. GTIN: 00300651356380 EA, 20300650357399 CS All lots received between 7/4/21-9/30/21

Distribution pattern

US Nationwide

device · product 9 of 55

Perifix LOR Syringe Perifix 8 mL Pouch Luer Lock Tip Without Safety Model Number: 332152

Z-1591-2022
Recall number
Z-1591-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
415 eaches

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: 04046964177613; 04046964177620

Distribution pattern

US Nationwide

device · product 10 of 55

B. Braun EVA Gravity Mixing Container 1000 mL Model Number: 2112363

Z-1592-2022
Recall number
Z-1592-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
1 Case

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: 04046964244926; 04046964244940; 04046964244933

Distribution pattern

US Nationwide

device · product 11 of 55

Ultracell Eye Pledget Ultracell 2 X 6 X 1 mm, Sterile Model Number: 40825

Z-1593-2022
Recall number
Z-1593-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
2 Box

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: 00886158012108; 30886158012109

Distribution pattern

US Nationwide

device · product 12 of 55

Wetfield Eraser Bipolar Hemostatic Eraser Wet-Field Eraser 23 Gauge Tapered Model Number: 221265

Z-1594-2022
Recall number
Z-1594-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
1 box

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: 00886158010524; 30886158010525

Distribution pattern

US Nationwide

device · product 13 of 55

Cadwell Disposable Ground Electrodes Grounding Pad 1.25 X 1.75 Inch Dimensions, Disposable Model Number: 302288-000

Z-1595-2022
Recall number
Z-1595-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
2 Boxes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: 20840067101395; 10840067101398; 00840067101391

Distribution pattern

US Nationwide

device · product 14 of 55

Excelsior Heparin Sodium, Porcine, Preservative Free 100 U / mL Solution Prefilled Syringe, Partial Fill 5 mL Fill in 10 mL Syringe Model Number: 513604

Z-1596-2022
Recall number
Z-1596-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
13 boxes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: 00363807600515; 10363807600055; 00363807600058

Distribution pattern

US Nationwide

device · product 15 of 55

MAGELLAN DIAGNOSTICS LeadCare II Blood Lead Test Kit Rapid Test Kit LeadCare II General Chemistry Blood Lead Test Whole Blood Sample 48 Tests Model Number: 70-6762

Z-1597-2022
Recall number
Z-1597-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
81 kits

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: 00850355006000

Distribution pattern

US Nationwide

device · product 16 of 55

Strep test: a. McKesson Medical-Surgical McKesson Rapid Test Kit McKesson Consult Infectious Disease Immunoassay Strep A Test Throat / Tonsil Saliva Sample 25 Tests, Model Number: 5003. b. QUIDEL Sofia TEST KIT, STREP A+ SOFIA (25/KT 12KT/CS) Model Number: 20274. c. Alere SAN DIEGO INC McKesson TEST, KIT STREP A DIPSTICK WAIVED (50/KT) Exempt Catalog #4999. d. In-Line Control Swab Quickvue In-Line Strep A Test Positive Level / Negative Level 12 Swabs (IVD) Catalog # 00345. e. (added 11/30/22) Abbott Rapid Test Kit Acceava Infectious Disease Immunoassay Strep A Test Throat Swab Sample 50 Tests, Model Number: 92001

Z-1598-2022
Recall number
Z-1598-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
a. 214 kits b. 1cs c. 53 kits d. 4 bx e. 1 KT

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: a. 00612479240100; 00612479202733. b. 30014613202745. c. 00612479202726; 612479240094. d. 30014613003458. e. 10815845020031, 00815845020034.

Distribution pattern

US Nationwide

device · product 17 of 55

a. MERIT MEDICAL SYSTEMS Aspira Dressing Kit Aspira Model Number: 4991503. b. MERIT MEDICAL SYSTEMS Aspira Pleural / Peritoneal Drainage Kit Aspira 1000 mL Sterile Model Number: 4992301.

Z-1599-2022
Recall number
Z-1599-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
a. 123 b. 407

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: a. 00884450394984 (EA); 00801741045011 (EA); 10801741045018 (CA); 10884450394981 (CA); 20801741045015 (BX); 20884450394988 (BX). b. 00801741045035 (EA); 00884450394861 (EA); 10801741045032 (CA); 10884450394868 (CA); 20801741045039 (BX); 20884450394865 (BX)

Distribution pattern

US Nationwide

device · product 18 of 55

MERIT MEDICAL SYSTEMS Temno Soft Tissue Biopsy Device Temno 14 Gauge 6 cm Length Beveled Sharp Tip Model Number: T146

Z-1600-2022
Recall number
Z-1600-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
8 Boxes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: 00884450444467; 20884450444461; 10884450444464

Distribution pattern

US Nationwide

device · product 19 of 55

a. MMS - IMMUNOSTICS INC McKesson Rapid Test Kit Consult Colorectal Cancer Screening Fecal Occult Blood Test (iFOB or FIT) Stool Sample 25 Tests, Model Number: 4487. b. MMS - IMMUNOSTICS INC McKesson Rapid Test Kit McKesson Consult Colorectal Cancer Screening Fecal Occult Blood Test (FOBT) Stool Sample 100 Tests Model Number: 4487. c. MMS - IMMUNOSTICS INC McKesson Rapid Test Kit McKesson Consult Colorectal Cancer Screening Fecal Occult Blood Test (FOBT) Stool Sample 50 Tests Model Number: 127-50ER

Z-1601-2022
Recall number
Z-1601-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
boxes: a. 20 b. 21 c. 4

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: a. 10612479219417; 20612479198368. b. 10612479226132; 20612479225569. c. 10612479226125; 20612479225552

Distribution pattern

US Nationwide

device · product 20 of 55

NANOSONICS LTD Sonex-HL Ultrasound Probe Disinfectant trophon Sonex-HL 80 mL Bottle For Trophon EPR Disinfection System Model Number: N00037

Z-1602-2022
Recall number
Z-1602-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
31 Boxes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: 09350855000061; 09350855000078; 09350855000023

Distribution pattern

US Nationwide

device · product 21 of 55

Palmero Healthcare, LLC DisCide Ultra Surface Disinfectant Cleaner Quaternary Based Manual Pour Liquid 1 gal. Jug Herbal Scent NonSterile Model Number: 3565G

Z-1603-2022
Recall number
Z-1603-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
8 Eaches

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: 00840415100212

Distribution pattern

US Nationwide

device · product 22 of 55

TELEFLEX LLC Arrow Central Venous Catheter Kit 16, 18 Gauge Multi Lumen Model Number:CDC-45703-XP1A (Model Numbers # IPN035619, IPN036437, IPN922677)

Z-1604-2022
Recall number
Z-1604-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
5 each

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: 30801902058615; 00801902058614; 20801902058618;

Distribution pattern

US Nationwide

device · product 23 of 55

STERIS CORP Revital-Ox Resert Hydrogen Peroxide High-Level Disinfectant Revital-Ox RESERT RTU Liquid 4 Liter Container Max 21 Day Reuse Model Number: 4455AW

Z-1605-2022
Recall number
Z-1605-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
20.25 CS

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: 00724995095017; 50724995095012

Distribution pattern

US Nationwide

device · product 24 of 55

a. ABBOTT RAPID DX N AMERICA LLC Alere Rapid Test Kit Alere Fertility Test hCG Pregnancy Test Urine Sample 30 Tests, Model Number: 92210. b. ABBOTT RAPID DX N AMERICA LLC Alere Rapid Test Kit Alere hCG Dipstick Fertility Test hCG Pregnancy Test Urine Sample 50 Tests Model Number: 92211.

Z-1606-2022
Recall number
Z-1606-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
a. 5 kits b. 12 kits

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: a. 10815845020130; 00815845020133. b. 10815845020093, 00815845020096

Distribution pattern

US Nationwide

device · product 25 of 55

GETINGE USA SALES LLC OCEAN Chest Drain System Atrium 2100 mL Model Number: 2002-000

Z-1607-2022
Recall number
Z-1607-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
6 each

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: 00650862100013; 20650862100017

Distribution pattern

US Nationwide

device · product 26 of 55

3M COMPANY 3M PAD, GROUNDING SAFETY RING Model Number: 9165

Z-1608-2022
Recall number
Z-1608-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
8 cases

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: 50707387462593; 00707387462598 EA

Distribution pattern

US Nationwide

device · product 27 of 55

MEDLINE INDUSTRIES Medline Catheter Insertion Tray Medline Foley Without Catheter Without Balloon Model Number: DYND10160

Z-1609-2022
Recall number
Z-1609-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
60 each

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: 10080196997091; 40080196997092

Distribution pattern

US Nationwide

device · product 28 of 55

MEDLINE INDUSTRIES Medline Plug, Catheter Medline Plastic, with Cover Model Number: DYND12200

Z-1610-2022
Recall number
Z-1610-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
1 Case

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: 10080196030873; 40080196030874

Distribution pattern

US Nationwide

device · product 29 of 55

MEDLINE INDUSTRIES Centurion IV Securement Kit Model Number: IVSSTK3

Z-1611-2022
Recall number
Z-1611-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
3 cases

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: 10653160244950 EA; 00653160244953 CS

Distribution pattern

US Nationwide

device · product 30 of 55

Fischer Cone Biopsy Excisor EXCISOR, CONE FISCHER BIOPSY WD ANGL SM (5/BX) Model Number: 900-157

Z-1612-2022
Recall number
Z-1612-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
5 each

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: 00888937003765; 20888937003769

Distribution pattern

US Nationwide

device · product 31 of 55

Mckesson GYNECATH H/S CATHETER 5FR (10/CS) Model Number: 11-19610

Z-1613-2022
Recall number
Z-1613-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
a. 30 each b. 0.3 cs

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: a. 20612479161539; 30612479162472 BX; 40612479161571 CS. b. 20612479161546; 30612479162489 BX; 40612479161588 CS

Distribution pattern

US Nationwide

device · product 32 of 55

a. McKesson DISINFECTANT, GLUTARALDEHYDE 28DAY (4GL/CS) MGM68, Model Number: 68-102800. b. METREX RESEARCH McKesson 14-Day Glutaraldehyde Solution DISINFECTANT, GLUTARALDEHYDE 14DAY (4GL/CS) MGM68 Model Number: 68-101400. c. METREX RESEARCH McKesson SOLUTION, GLUT 2.5% 28DAY QT (16/CS) PSS744 Catalog # 341. d. METREX RESEARCH LLC MetriCide DISINFECTANT, METRICIDE 14DAYGLUTARALDEHYDE 1GL (4/CS) Catalog # 10-1400. e. METREX RESEARCH LLC MetriCide28 DISINFECTANT, METRICIDE GLUT LNG LIFE GL (4GL/CS) Catalog # 10-2800

Z-1614-2022
Recall number
Z-1614-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
28 gallons b. 38 gal c. 16 qt d. 40 gal e. 124 gal

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: a. 10612479150581; 40612479150599 CS. b. 10612479150567; 40612479150575 CS. c. 10612479204406; 40612479204414. d. 00615375005453; 10615375005450 CS; H9711014002. e. 00615375005477; 10615375005474 CS; H97110280022

Distribution pattern

US Nationwide

device · product 33 of 55

MedSource IV Start kit, 8inch Extension Set IV START KIT, W/SITE LOC/8" EX100/CS Model Number: MS-80047

Z-1615-2022
Recall number
Z-1615-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
53 each

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: 00816703021811

Distribution pattern

US Nationwide

device · product 34 of 55

B. BRAUN MEDICAL INC. Anesthesia Support Tray SUPPORT TRAY, +EXT SET(10/CS)ST200E Model Number: 332116

Z-1616-2022
Recall number
Z-1616-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
16 cases

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: 04046964177538; 04046964177545

Distribution pattern

US Nationwide

device · product 35 of 55

a. BECTON DICKINSON BD Vacutainer C&S Preservative Urine Tube TUBE, URINE COLL PLAS 4ML (100/BX 10BX/CS), Model Number: BD 364951. b. BECTON DICKINSON BD Vacutainer C&S Transfer Straw Kit TRANSFER STRAW KIT, URINE 4ML(50/BX 4BX/CS) Model Number: BD 364953. c. BECTON DICKINSON BD Vacutainer COLLECTION KIT, URINE COMPLETE 8ML 13"X75" (50/CS) BD Model Number: 364957

Z-1617-2022
Recall number
Z-1617-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
a. 25 bx b. 53 bx c. 31 cs

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: a. 00382903649518 EA; 30382903649519 PK; 50382903649513. b. 00382903649532; 30382903649533; 50382903649537. c. 00382903649570 EA; 50382903649575 CS

Distribution pattern

US Nationwide

device · product 36 of 55

a. BECTON DICKINSON BD Vacutainer SST TUBE, BLD COL CLOT/SEP GLD 3.5ML PLAS VACUTAINER (100/BX), Model Number: 367983. b. BECTON DICKINSON BD Vacutainer SST TUBE, BLD COL CLOT/SEP RED/GRY8.5ML PLAS VACUTAINER (100/BX Model Number: 367988. c. BECTON DICKINSON BD Vacutainer SST TUBE, BLD COL CLOT/SEP GLD 5MLPLAS VACUTAINER (100/BX) Model Number: 367986. d. BECTON DICKINSON BD Vacutainer SST TUBE, BLD COL CLOT/SEP RED/GRY7.5ML PLAS VACUTAINER (100/BX) Model Number: 367987. e. BECTON DICKINSON BD Vacutainer SST TUBE, BLD COL CLOT/SEP RED/GRY3.5ML PLAS VACUTAINER (100/BX Model Number: 367981. f. BECTON DICKINSON BD Vacutainer TUBE, BLD COL PLAIN RED 10ML GLS VACUTAINER (100/BX 10BX/CS) Model Number: 366430. g. BECTON DICKINSON BD Microtainer SST - Amber TUBE, CAPILLARY CLOT/SEP GLD 400/600UL PLAS MICROT (50/BX) Model Number: 365978. h. BECTON DICKINSON BD Vacutainer CPT NC: 1.0mL FICOLL: 2.0mL TUBE, BLD CPT SOD CIT 8ML (60/CS) Model Number: BD 362761. i. BECTON DICKINSON BD Vacutainer Rapid Serum Tube (RST) Thrombin TUBE, BLD COL CLOT ORG 5ML PETVACUTAINER (100/BX 10BX/CS) Model Number: 368774. j. BECTON DICKINSON BD Vacutainer Buff. Na Citrate 0.109M, 3.2% TUBE, BLD COL SODCIT LTBLU 2.7ML PLAS VACUTAINER (100/BX) Model Number: 363083.

Z-1618-2022
Recall number
Z-1618-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
a. 67 boxes b. 131 c. 51 d. 121 e. 2 f. 38 g. 16 h. 240 i. 17 j. 41

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: a. 00382903679836; 50382903679831. b. 00382903679881; 50382903679886. c. 00382903679867; 50382903679862. d. 00382903679874; 50382903679879, e. 00382903679812; 50382903679817. f. 00382903664306; 30382903664307; 50382903664301. g. 00382903659784; 50382903659789. h. 00382903627615; 50382903627610. i. 00382903687749; 50382903687744. j. 00382903630837; 50382903630832.

Distribution pattern

US Nationwide

device · product 37 of 55

a. Medefil Normal Saline IV Flush Syringe NORMAL SALINE FLUSH, SYR 10ML/12ML (60/BX 16BX/CS), Model Number: MIS-1130. b. MEDEFIL INC McKesson SALINE IV FLUSH, SYR NORMAL 10ML/12ML .9% (60/BX 16BX/CS) Model Number: 191-MIS-1130.

Z-1619-2022
Recall number
Z-1619-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
a. 20 Boxes b. 1 bx

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: a. 10364253111300; 50364253000305; 30364253111304. b. 10612479247670; 40612479247695; 20612479247684.

Distribution pattern

US Nationwide

device · product 38 of 55

a. METREX RESEARCH CORP CaviCide1 DISINFECTANT, CLNR CAVICIDE1 1GL (4/CS) METREX, Model Number: 13-5000. b. METREX RESEARCH CORP CaviCide DISINFECTANT, CAVICIDE 8OZ SPRAY MX-1008 METREX Model Number: 13-1008. c. METREX RESEARCH CORP CaviCide DISINFECTANT, CAVICIDE GL MX-1000 METREX Catalog #13-1000. d. METREX RESEARCH CORP CaviCide DISINFECTANT, CAVICIDE PUMP SPRAY 24OZ METREX Catalog #13-1024. e. CaviCide1 DISINFECTANT, CLNR CAVICIDE1 24OZ (12/CS) METREX Catalog #13-5024. f. METREX RESEARCH CORP DISINFECTANT, ENVIROCIDE 24OZ(12/CS) METREX Model Number: 13-3324. g. METREX RESEARCH CORP Envirocide DISINFECTANT, ENVIROCIDE GL(4/CS)MX-3300 METREX Model Number: 13-3300

Z-1620-2022
Recall number
Z-1620-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
50cs b. 38 c. 519gal d. 1671 e. 43.25cs f. 33btl g. unk

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: a. 00615375005446; H97113500020. b. 00615375005309; H97113100824. c. 00615375005385; H9711310002. d. 00615375005361, H97113102422. e. 00615375005415, H97113502426. f. 00615375005354; H97113332427. g. 00615375005378; H113330021

Distribution pattern

US Nationwide

device · product 39 of 55

METREX RESEARCH CORP SPONGE, METRISPONGE W/METRIZYME (25/BX 4BX/CS) Model Number: 10-4025

Z-1621-2022
Recall number
Z-1621-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
5 Boxes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: 00615375006771; 00615375003671

Distribution pattern

US Nationwide

device · product 40 of 55

Dynarex¿ PAD, NAIL POLISH REMOVER (100/BX 10BX/CS) DYNREX Catalog # 1501

Z-1622-2022
Recall number
Z-1622-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
2 Boxes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: Not Available

Distribution pattern

US Nationwide

device · product 41 of 55

a. DERMA SCIENCES, INC. NG Strip FASTENER, NASAL TUBE IND WRAP(25/BX), Catalog NG25. b. DERMA SCIENCES, INC. Surgitube BANDAGE, GAUZE #2P 7/8"X50YDS DERSCI Catalog GL-242. c. DERMA SCIENCES, INC. Surgilast TUBE NET SZ3 MED 10YDS/EA HAND, ARM, LEG, FOOT SURGILAST Catalog # GL103. d. DERMA SCIENCES, INC. Surgitube & Surgigrip APPLICATOR, SURGITUBE/GRIP METAL SZ3 6" CHLD/ADLT DERSCI Catalog #GL-234.

Z-1623-2022
Recall number
Z-1623-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
a. 772 b. 9 c. 1 d. 1

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

a. GTIN: 00753567101252; 10753567101259. b. GTIN: 809958001158. c. GTIN: Not Available. d. GTIN: unknown

Distribution pattern

US Nationwide

device · product 42 of 55

FISHER SCIENTIFIC Sure-Vue PIPETTE, RPR DISPENSING (500/PK) Catalog # 23038015

Z-1624-2022
Recall number
Z-1624-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
3 pk

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

Not Available

Distribution pattern

US Nationwide

device · product 43 of 55

BEAVER-VISITEC INTERNATIONAL, INC. Ultracell WICK, FENSTD PED 7MMX20MM(10/BX) BVRVIS Catalog #30316-C

Z-1625-2022
Recall number
Z-1625-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
3 Boxes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

Not Available

Distribution pattern

US Nationwide

device · product 44 of 55

BEAVER-VISITEC INTERNATIONAL, INC. Visitec CANNULA, LASIK IRR (10/BX)BVRVIS Catalog #585278

Z-1626-2022
Recall number
Z-1626-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
1 Box

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: 30886158002995; 00886158002994 EA

Distribution pattern

US Nationwide

device · product 45 of 55

FISHER SCIENTIFIC Fisherbrand SWAB TRANS STUARTS DBL 50BX Catalog #1490721

Z-1627-2022
Recall number
Z-1627-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
25 Boxes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
XXX

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

XXX

Code information

Unknown

Distribution pattern

US Nationwide

device · product 46 of 55

FISHER SCIENTIFIC Aseptic Control¿ LUBRICATING JELLY PAP TEST 4OZ(12/PK) Catalog #22998006

Z-1628-2022
Recall number
Z-1628-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
7 packs

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

Not available

Distribution pattern

US Nationwide

device · product 47 of 55

BECKMAN COULTER, INC. a. COULTER DxH Diff Pack REAGENT, DIFF PK FP DXHCOULTR, Catalog #628020. b. COULTER DxH Cleaner REAGENT, CLEANER FP DXH 10LCOULTR Catalog #628023. c. DxH 500 Series Lyse LYSE, VERSA SOL DXH 500 SERIES(0.5L/KT) Catalog # B36846. d. DxH 500 Series Cleaner CLEANER, COULTER CLENZ DXH 500SERIES (0.5L/KT) Catalog # B36868

Z-1629-2022
Recall number
Z-1629-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
a. 11 b. 13 c. 15 d. 33

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: a. 15099590233716. b. 15099590233747. c. 15099590671860. d. 15099590671877

Distribution pattern

US Nationwide

device · product 48 of 55

CENTURION MEDICAL PRODUCTS, LP Centurion CATH KIT, FML W/LUBE 8FR (50/CS) CNTURN Catalog # CKF105L

Z-1630-2022
Recall number
Z-1630-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: 00653160044300, 50653160044305

Distribution pattern

US Nationwide

device · product 49 of 55

COOPER SURGICAL Milex PESSARY, RING MILEX INCONT FLEXIBLE SZ6 1 3/4" Catalog # MXPCON06

Z-1631-2022
Recall number
Z-1631-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
1 each

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: 888937004427

Distribution pattern

US Nationwide

device · product 50 of 55

MORRISON MEDICAL Morrison Medical OB KIT, HARD PK SEALED W/CARDBOARD BX MORMED Catalog #0967NL

Z-1632-2022
Recall number
Z-1632-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
16 each

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: 00647921096707

Distribution pattern

US Nationwide

device · product 51 of 55

DYNAREX Dynarex SWABSTICK, PVP (3/PK 25/BX 10BX/CS) Catalog #1202

Z-1633-2022
Recall number
Z-1633-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
197 boxes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: Not available

Distribution pattern

US Nationwide

device · product 52 of 55

Dynarex SWAB, LEMON GLYCERIN (3/PK 25PK/BX 10BX/CS) DYNREX Catalog # 1216

Z-1634-2022
Recall number
Z-1634-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
135.08 boxes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: Not available

Distribution pattern

US Nationwide

device · product 53 of 55

DYNAREX DynaLube LUBRICATING JELLY, STR 2.7GM (144/BX 12BX/CS) Catalog #1250

Z-1635-2022
Recall number
Z-1635-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
17.5 boxes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: 00616784125039; 00616784125015; '00616784125022

Distribution pattern

US Nationwide

device · product 54 of 55

FISHER SCIENTIFIC Fisherbrand SWAB, ROUND BOTTOM CLR (50/PK)FSHSCI Catalog # 1490712

Z-1636-2022
Recall number
Z-1636-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
154 pack

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: Unknown

Distribution pattern

US Nationwide

device · product 55 of 55

MEDICAL CHEMICAL CORPORATION Total-Fix STOOL COLL KIT, TOTAL FIX PARASITOLOGY (100/CS) Catalog # NC0585129

Z-1637-2022
Recall number
Z-1637-2022
Initiated
May 25, 2022
Classification
Class II
Status
Ongoing
Quantity
1 case

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Code information

GTIN: Unknown

Distribution pattern

US Nationwide