Medline Industries recalls specific lots of Neuro Pack-LF Convenience kits due to potential endotoxin levels in surgical materials. Affected kits may pose a risk during medical procedures. Contact Medline for details.
Surgical Patties & Surgical Strips in specific lots of Custom Convenience Kits were found to contain higher-than-expected levels of endotoxin within the raw material used to produce sterile Codman Surgical Patties and Strips that may have resulted in out-of-specification levels of endotoxin in those finished goods
Medline Industries is recalling specific lots of Neuro Pack-LF Convenience kits because they may contain higher-than-expected endotoxin levels. This could affect surgical safety during medical procedures if the kits are used improperly.
The kits contain surgical patties and strips that may have higher-than-expected endotoxin levels from the raw materials. Endotoxins are bacterial components that can cause infections or adverse reactions if introduced into the body during medical procedures.
Healthcare professionals using the Neuro Pack-LF Convenience kits for surgical procedures are most at risk. Patients receiving these kits during medical procedures may also be affected.
Check for the lot number 23AMD730 on the packaging. The product is sold under SKU DYNJ0578916X with UDI-DI numbers 10193489288384 (each) or 40193489288385 (case).
Look for the lot number 23AMD730 on the packaging or check the UDI-DI numbers 10193489288384 (each) or 40193489288385 (case).
The specific lot number for this recall is 23AMD730.
Check for the lot number 23AMD730 on the packaging or verify the UDI-DI numbers 10193489288384 (each) or 40193489288385 (case).
The recall record does not specify a remedy, so contact Medline Industries directly for further instructions.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-0717-2025 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-0717-2025 from Medline Industries. 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.
