Cardinal Health recalls Presource Laryngoscopy Packs with potential endotoxin contamination in non-sterile surgical strips. Affected kits include specific catalog numbers and lot numbers. Consumers should contact Cardinal Health for details.
Potential endotoxin contamination in non-sterile surgical strips and patties in Presource kits.
Cardinal Health is recalling several laryngoscopy packs due to potential endotoxin contamination in non-sterile surgical strips. This could pose a risk of infection or complications during medical procedures if used improperly.
Endotoxins are bacterial components that can cause infections or adverse reactions when introduced into the body. Non-sterile surgical strips in these kits may contain endotoxins, potentially leading to infections or complications during medical procedures.
Healthcare professionals using the Presource Laryngoscopy Packs for medical procedures are most at risk. Patients undergoing surgery with these kits could face infection risks if the endotoxin contamination occurs.
Check for catalog numbers SEN11LGUH2 through SEN11LGUHB and specific lot numbers listed in the recall notice. These kits were sold with the described catalog numbers and lot numbers.
Reach out to Cardinal Health directly for specific instructions on how to return or replace the affected Presource Laryngoscopy Packs.
The affected catalog numbers are SEN11LGUH2, SEN11LGUH3, SEN11LGUH4, SEN11LGUH5, and SEN11LGUHB.
Check the catalog number and lot number on your Presource Laryngoscopy Pack against the list provided in the recall notice.
The recall states potential endotoxin contamination, which could lead to infection or complications, but the hazard level is low risk as no specific injury mechanism is described.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-0912-2025 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-0912-2025 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.
