Reported Jan 22, 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?

317 of 317 products

Products covered by this recall
Model / numberBarcodesProduct as published
1088843901137150888439011379Catalog Number PGVMFFBLY, UDI/DI 10888439011371 (EA)50888439011379 (CS), Lot Number J34J41
1088843901137150888439011379Catalog Number PGVMFFBLY, UDI/DI 10888439011371 (EA)50888439011379 (CS), Lot Number J43U77
1088843964193650888439641934Catalog Number PGVMFFBLZ, UDI/DI 10888439641936 (EA)50888439641934 (CS), Lot Number J4952G
1088843964193650888439641934Catalog Number PGVMFFBLZ, UDI/DI 10888439641936 (EA)50888439641934 (CS), Lot Number J53W73
1088843964193650888439641934Catalog Number PGVMFFBLZ, UDI/DI 10888439641936 (EA)50888439641934 (CS), Lot Number J4952H
1088843964193650888439641934Catalog Number PGVMFFBLZ, UDI/DI 10888439641936 (EA)50888439641934 (CS), Lot Number J6050F
1088843964193650888439641934Catalog Number PGVMFFBLZ, UDI/DI 10888439641936 (EA)50888439641934 (CS), Lot Number J74A27
1088843964193650888439641934Catalog Number PGVMFFBLZ, UDI/DI 10888439641936 (EA)50888439641934 (CS), Lot Number J7963D
1088843964193650888439641934Catalog Number PGVMFFBLZ, UDI/DI 10888439641936 (EA)50888439641934 (CS), Lot Number J7905F
1088843964193650888439641934Catalog Number PGVMFFBLZ, UDI/DI 10888439641936 (EA)50888439641934 (CS), Lot Number J84K02
1088843964193650888439641934Catalog Number PGVMFFBLZ, UDI/DI 10888439641936 (EA)50888439641934 (CS), Lot Number J8692Y
1088843964193650888439641934Catalog Number PGVMFFBLZ, UDI/DI 10888439641936 (EA)50888439641934 (CS), Lot Number J86T82
PN23SPAM51019559423560450195594235602UDI/DI 10195594235604 (EA)50195594235602 (CS), Lot Number 20166041-3014
PN23SPAM51019559423560450195594235602UDI/DI 10195594235604 (EA)50195594235602 (CS), Lot Number 5138318
PN33MSOC31019710666088150197106660889UDI/DI 10197106660881 (EA)50197106660889 (CS), Lot Number 7331471
PN33MSOCH1019710647349850197106473496UDI/DI 10197106473498 (EA)50197106473496 (CS), Lot Number 7265882
PN33MSOCH1019710647349850197106473496UDI/DI 10197106473498 (EA)50197106473496 (CS), Lot Number 7280085
PN33MSOCI1019710658652550197106586523UDI/DI 10197106586525 (EA)50197106586523 (CS), Lot Number 7265980
PN40LMBY61019559405957650195594059574UDI/DI 10195594059576 (EA)50195594059574 (CS), Lot Number J9601U
PN40LMBY61019559405957650195594059574UDI/DI 10195594059576 (EA)50195594059574 (CS), Lot Number J96A01
Amount recalled
512,786 total units

This recall covers 10 products

The agency filed one notice per product. You are reading one of them; the other 9 are below.

Where it was sold

  • Nationwide

Why it was recalled

Potential 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 Sep 19, 4:57 PM 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.