Reported Feb 19, 2025 · Ongoing

Cardinal Health Presource Kits

Cardinal Health 200, LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Cardinal Health 200, LLC · 3651 Birchwood Dr · Waukegan, IL · 60085-8337

Is this the product you have?

Cardinal Health Presource Kits

64 of 64 products

Products covered by this recall
Model / numberProduct as published
PB23DFCM3KIT,DIEP FLAP
PB23DFCM4KIT,DIEP FLAP
PB23DFCM5KIT,DIEP FLAP
PB23DFCM6KIT,DIEP FLAP
PB23DFCM7KIT,DIEP FLAP
PB23DFCMAKIT,DIEP FLAP
PE40HNAJ10KIT, HEAD AND NECK
PE40HNAJ11KIT, HEAD AND NECK
PE40HNAJ12KIT, HEAD AND NECK
PE40HNAJ13KIT, HEAD AND NECK
PE40HNAJ14KIT, HEAD AND NECK
PE40HNAJ15KIT, HEAD AND NECK
PE40HNAJ16KIT, HEAD AND NECK
PE40HNAJ17KIT, HEAD AND NECK
PE40HNAJ18KIT, HEAD AND NECK
PE40HNAJ19KIT, HEAD AND NECK
PE40HNAJ20KIT, HEAD AND NECK
PE40HNAJU1KIT, HEAD AND NECK
PE40HNAJU2KIT, HEAD AND NECK
PE40HNAJU3KIT, HEAD AND NECK
Lot codes and dates

328 of 328 products

Products covered by this recall
Model / numberBarcodesProduct as published
—1088843958705050888439587058PB23DFCM3, UDI-DI:10888439587050 (each) 50888439587058 (case), Lot Number: J37U13
—1088843960105350888439601051PB23DFCM4, UDI-DI:10888439601053 (each) 50888439601051 (case), Lot Number: J37U14
—1088843964179050888439641798PB23DFCM5, UDI-DI:10888439641790 (each) 50888439641798 (case), Lot Number: J46C08
—1088843983617250888439836170PB23DFCM6, UDI-DI:10888439836172 (each) 50888439836170 (case), Lot Number: J6050A
—1088843985308750888439853085PB23DFCM7, UDI-DI:10888439853087 (each) 50888439853085 (case), Lot Number: J7704J
—1088748853129850887488531296PB23DFCMA, UDI-DI:10887488531298 (each) 50887488531296 (case), Lot Number: J4952P
—1088748853129850887488531296PB23DFCMA, UDI-DI:10887488531298 (each) 50887488531296 (case), Lot Number: J53W77
—1088748853129850887488531296PB23DFCMA, UDI-DI:10887488531298 (each) 50887488531296 (case), Lot Number: J5679N
—1088748853129850887488531296PB23DFCMA, UDI-DI:10887488531298 (each) 50887488531296 (case), Lot Number: J84K06
—1088748853129850887488531296PB23DFCMA, UDI-DI:10887488531298 (each) 50887488531296 (case), Lot Number: J85W31
—1019559474651350195594746511PE40HNAJ10, UDI-DI:10195594746513 (each) 50195594746511 (case), Lot Number: 5918338
—1019559477768550195594777683PE40HNAJ11, UDI-DI:10195594777685 (each) 50195594777683 (case), Lot Number: 6279857
—1019559480805150195594808059PE40HNAJ12, UDI-DI:10195594808051 (each) 50195594808059 (case), Lot Number: 5649225
—1019559487867250195594878670PE40HNAJ13, UDI-DI:10195594878672 (each) 50195594878670 (case), Lot Number: 6279859
—1019710605790250197106057900PE40HNAJ14, UDI-DI:10197106057902 (each) 50197106057900 (case), Lot Number: 6487892
—1019710611644950197106116447PE40HNAJ15, UDI-DI:10197106116449 (each) 50197106116447 (case), Lot Number: 6487896
—1019710613863250197106138630PE40HNAJ16, UDI-DI:10197106138632 (each) 50197106138630 (case), Lot Number: 5
—1019710613863250197106138630PE40HNAJ16, UDI-DI:10197106138632 (each) 50197106138630 (case), Lot Number: 6560940
—1019710622420550197106224203PE40HNAJ17, UDI-DI:10197106224205 (each) 50197106224203 (case), Lot Number: 6568677
—1019710648016850197106480166PE40HNAJ18, UDI-DI:10197106480168 (each) 50197106480166 (case), Lot Number: 7197963
Amount recalled
973,785 total units

This recall covers 12 products

The agency filed one notice per product. You are reading one of them; the other 11 are below.

Where it was sold

  • Nationwide

Why it was recalled

Potential for endotoxin contamination in non-sterile surgical strips and patties in Presource Kits.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Nov 4, 10:17 AM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.