Cardinal Health recalls Presource Kits with potential endotoxin contamination in non-sterile surgical strips and patties. Affected kits include specific catalog numbers and lot numbers. Consumers should contact Cardinal Health for details.
Potential for endotoxin contamination in non-sterile surgical strips and patties in Presource Kits.
Cardinal Health is recalling certain Presource Kits due to potential endotoxin contamination in non-sterile surgical strips and patties. This could pose a risk of infection or other health issues if used in medical procedures.
Endotoxins are bacterial components that can cause infections when introduced into the body. Non-sterile surgical strips and patties in these kits may contain endotoxins, potentially leading to infections if used in medical procedures.
Healthcare professionals and surgical teams using the recalled Presource Kits are most at risk. Patients receiving procedures with these kits could be affected if the endotoxin contamination leads to infection.
Check for catalog numbers PN76LMM14, PN76LMMD9, or PN76LMMDX on the kit packaging. Look for lot numbers J8241D, J79Z55, J4220A, J4220D, J4953F, or J46C13.
Verify the catalog number and lot number on the Presource Kit packaging to determine if it is affected.
The hazard is potential endotoxin contamination in non-sterile surgical strips and patties, which could lead to infections if used in medical procedures.
Check for catalog numbers PN76LMM14, PN76LMMD9, or PN76LMMDX and lot numbers J8241D, J79Z55, J4220A, J4220D, J4953F, or J46C13.
Contact Cardinal Health directly for instructions on how to handle the affected kit, as the recall remedy is not specified in the record.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-1127-2025 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-1127-2025 from Cardinal Health. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
