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?
337 of 337 products
| Model / number | Barcodes | Product as published |
|---|---|---|
PGHDOT951 | 1088843969222850888439692226 | UDI/DI 10888439692228 (EA)50888439692226 (CS), Lot Number J4952D |
PGHDOT952 | 1088843982126050888439821268 | UDI/DI 10888439821260 (EA)50888439821268 (CS), Lot Number J6050F |
PWHDOT910 | 1019710643505250197106435050 | UDI/DI 10197106435052 (EA)50197106435050 (CS), Lot Number 6788561 |
PWHDOT911 | 1019710664672450197106646722 | UDI/DI 10197106646724 (EA)50197106646722 (CS), Lot Number 7332903 |
PWHDOT912 | 1019710667319550197106673193 | UDI/DI 10197106673195 (EA)50197106673193 (CS), Lot Number 7163082 |
PWHDOT913 | 1019710671336550197106713363 | UDI/DI 10197106713365 (EA)50197106713363 (CS), Lot Number 7332912 |
PWHDOT914 | 1019710671883450197106718832 | UDI/DI 10197106718834 (EA)50197106718832 (CS), Lot Number 7332914 |
PWHDOT951 | 1088843994017650888439940174 | UDI/DI 10888439940176 (EA)50888439940174 (CS), Lot Number J84K02 |
PWHDOT952 | 1019559433147450195594331472 | UDI/DI 10195594331474 (EA)50195594331472 (CS), Lot Number J6278U |
PWHDOT953 | 1019559450549350195594505491 | UDI/DI 10195594505493 (EA)50195594505491 (CS), Lot Number 5664102 |
PWHDOT954 | 1019559455555950195594555557 | UDI/DI 10195594555559 (EA)50195594555557 (CS), Lot Number 5664101 |
PWHDOT955 | 1019559464613450195594646132 | UDI/DI 10195594646134 (EA)50195594646132 (CS), Lot Number 5891310 |
PWHDOT956 | 1019559469788450195594697882 | UDI/DI 10195594697884 (EA)50195594697882 (CS), Lot Number 5891313 |
PWHDOT957 | 1019710612998250197106129980 | UDI/DI 10197106129982 (EA)50197106129980 (CS), Lot Number 6563987 |
PWHDOT958 | 1019710618809550197106188093 | UDI/DI 10197106188095 (EA)50197106188093 (CS), Lot Number 6563989 |
PWHDOT959 | 1019710632977150197106329779 | UDI/DI 10197106329771 (EA)50197106329779 (CS), Lot Number 6701853 |
PWHDOT95A | 1088843974952650888439749524 | UDI/DI 10888439749526 (EA)50888439749524 (CS), Lot Number J8671K |
PWHDOT95A | 1088843974952650888439749524 | UDI/DI 10888439749526 (EA)50888439749524 (CS), Lot Number J8671M |
PWHDOT95A | 1088843974952650888439749524 | UDI/DI 10888439749526 (EA)50888439749524 (CS), Lot Number J8671P |
PWHDOT95C | 1088843998326550888439983263 | UDI/DI 10888439983265 (EA)50888439983263 (CS), Lot Number J86T83 |
- 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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