Medline recalls specific lots of DIEP Flap Convenience kits due to potential endotoxin levels in surgical materials. Affected kits may pose health risks during procedures. Consumers should check lot numbers and 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 is recalling specific lots of DIEP Flap Convenience kits because surgical materials in those kits may have higher-than-expected endotoxin levels. This could lead to health risks during medical procedures if the kits are used improperly.
Surgical patties and strips in specific lots contain higher-than-expected endotoxin levels from raw materials. This could lead to health risks during medical procedures if the kits are used without proper sterilization.
Medical professionals using DIEP Flap Convenience kits for surgical procedures are most at risk. Patients receiving these kits may also be affected if the kits are used in procedures where endotoxin levels are critical.
Check for lot number 24CMH776 on the DIEP Flap Convenience kit (SKU DYNJ910120). The kit was sold with UDI-DI numbers 10195327589202 and 40195327589203.
Look for lot number 24CMH776 on the DIEP Flap Convenience kit (SKU DYNJ910120).
Lot number 24CMH776.
Check for lot number 24CMH776 on the DIEP Flap Convenience kit (SKU DYNJ910120).
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-0719-2025 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-0719-2025 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.
