Cardinal Health recalls Presource Kits (Laryngoscopy Pack) with catalog number SRIET0979N due to potential endotoxin contamination in non-sterile surgical strips and patties. Affected units include specific lot numbers.
Potential for endotoxin contamination in non-sterile surgical strips and patties in Presource Kits.
Cardinal Health is recalling Presource Kits (Laryngoscopy Pack) with catalog number SRIET0979N because they may contain endotoxins in non-sterile surgical strips and patties. This could pose a risk of infection or complications during medical procedures.
Endotoxins are bacterial components that can cause infections or adverse reactions when introduced into the body. Non-sterile surgical strips and patties in these kits may contain endotoxins, potentially leading to infections or complications during medical procedures.
Healthcare professionals using these kits in medical settings are most at risk. Patients undergoing procedures with these kits could be exposed to endotoxins.
Check for catalog number SRIET0979N on the Presource Kits. Affected units include specific lot numbers: J4219A, J4678M, J53W13, J6277W, J7904P, J8491U, J6785Z, J6786D, J9602P, J96A00, J96N37, 5136008, and 5405613.
Look for the lot number on the Presource Kit packaging to determine if it is affected.
The catalog number is SRIET0979N.
Affected lot numbers include J4219A, J4678M, J53W13, J6277W, J7904P, J8491U, J6785Z, J6786D, J9602P, J96A00, J96N37, 5136008, and 5405613.
Check the lot number on the Presource Kit packaging; affected units have specific lot numbers listed in the recall notice.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-1131-2025 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-1131-2025 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.