Medline recalls specific lots of FESS-MB Pack-LF Convenience kits due to potential endotoxin levels in surgical materials. Affected kits may pose health risks during medical procedures.
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 is recalling certain lots of FESS-MB Pack-L: Convenience kits used in medical procedures because they may contain higher-than-expected endotoxin levels. This could lead to health risks during surgery or medical treatments.
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 FESS-MB Pack-LF Convenience kits for surgical procedures are most at risk. Patients undergoing surgery with these kits may also be affected.
Check for the lot number 23HMB316 on the kit. The product is sold under SKU DYNJ0888159I and has a UDI-DI code of 10195327050146 (each) or 40195327050147 (case).
Look for the lot number 23HMB316 on the FESS-MB Pack-LF Convenience kit.
The lot number for this recall is 23HMB316.
Check for the lot number 23HMB316 on the FESS-MB Pack-LF Convenience kit, which has SKU DYNJ0888159I and UDI-DI codes 10195327050146 (each) or 40195327050147 (case).
The recall record does not specify a remedy, so contact Medline Industries 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-0718-2025 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-0718-2025 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.
