Cardinal Health recalls 11 surgical kit types due to unexpected endotoxin variability in Medicom Ritmed Neurological Sponges, which could pose risks during procedures.
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
Cardinal Health is recalling 11 types of surgical kits because the sponges inside them have unexpected endotoxin levels. This could cause complications during medical procedures if the sponges are used without proper testing.
The sponges contain Medicom Ritmed Neurological Sponges with unexpected endotoxin variability. Endotoxins are bacterial components that can cause infections or immune reactions if not properly controlled during medical procedures.
Healthcare professionals using these surgical kits are most at risk. Patients undergoing procedures with these kits may be affected if the sponges are used without proper testing.
Check for the catalog numbers listed: SEN73NSKCF, SNE30CNOHE, SNE30CRJGY, SNE43NEE13, SNE5CLPB13, SNE69PSKR4, SNE7CSHY15, SNE7CSHY16, and SOP30ODSCL. These kits were sold with specific lot numbers and UDI-DI codes.
Identify the kit by checking the catalog numbers listed in the recall notice: SEN73NSKCF, SNE30CNOHE, SNE30CRJGY, SNE43NEE13, SNE5CLPB13, SNE69PSKR4, SNE7CSHY15, SNE7CSHY16, or SOP30ODSCL.
The recall is due to unexpected variability in endotoxin levels in Medicom Ritmed Neurological Sponges, which could pose risks during medical procedures.
The recall notice does not specify a remedy, so healthcare professionals should check the catalog numbers and contact Cardinal Health for further instructions.
Yes, the kits were sold with specific lot numbers such as 3024-2, 93845, 4730, and others 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-2946-2026 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-2946-2026 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.
