Cardinal Health recalls 35 Presource Kits for potential endotoxin contamination in non-sterile surgical strips and patties. Affected items include specific catalog numbers and lot numbers.
Potential for endotoxin contamination in non-sterile surgical strips and patties in Presource Kits.
Cardinal Health is recalling 35 different Presource Kits due to potential endotoxin contamination in non-sterile surgical strips and patties. This could pose a risk of infection or complications during medical procedures if used improperly.
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 or complications during surgery if used without proper sterilization.
Healthcare professionals and medical facilities that use these Presource Kits for surgical procedures. Patients undergoing surgery with contaminated kits could face infection risks.
Check for catalog numbers starting with PWV2MF104 through PWV2MFCPF in the Presource Kits. Lot numbers listed in the recall include J46C10, J8998R, and others. These kits were sold to healthcare facilities.
Look for catalog numbers from PWV2MF104 to PWV2MFCPF on the Presource Kits.
Check the lot number on the kit, which may be J46C10, J8998R, or other specific numbers listed in the recall.
The recall states there is a potential for endotoxin contamination in non-sterile surgical strips and patties within these kits.
Check the catalog number (PWV2MF104 to PWV2MFCPF) and lot number (e.g., J46C10, J8998R) as listed in the recall notice.
The recall does not specify a stop-use action, so users should check if their kits are affected before deciding to discard or return them.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-1130-2025 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-1130-2025 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.
