Cardinal Health recalls 329 Presource Kits for potential endotoxin contamination in non-sterile surgical strips and patties. Affected kits include specific catalog numbers and lot numbers. Stop using immediately to avoid infection risks.
Potential for endotoxin contamination in non-sterile surgical strips and patties in Presource Kits.
Cardinal Health is recalling 329 different Presource Kits due to potential endotoxin contamination in non-sterile surgical strips and patties. This could lead to infections if used in surgery. Affected kits have specific catalog numbers and lot numbers listed in the recall.
Endotoxins are bacterial components that can cause infections when introduced into the body. These kits are intended for surgical use but may contain non-sterile materials that could lead to infections if used improperly.
Surgical teams and medical facilities that own or use these Presource Kits are most at risk. Patients using the kits during surgery could face infection risks if the contamination occurs.
Check for catalog numbers like PE29NSFG4, PE29NSFG5, and others listed in the recall. Also look for specific lot numbers associated with each catalog number.
Discontinue use of all affected Presource Kits to prevent potential infection risks.
Affected kits include catalog numbers PE29NSFG4 through PE29NSFGN, PE36ESCHA, PECGOTSN1 through PECGOTSNE, and others listed in the recall with specific lot numbers.
Check the catalog number and lot number on your kit. The recall lists specific catalog numbers and corresponding lot numbers for affected items.
The recall states potential endotoxin contamination, which could lead to infections. However, the hazard is described as non-sterile materials, not a direct risk of serious injury in normal use.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-1132-2025 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-1132-2025 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
