Medline recalls custom medical procedure kits with non-sterile surgical patties and strips that may contain endotoxins. Affected kits include specific models and lot numbers. Consumers should check their kits and contact Medline for details.
Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
Medline is recalling custom medical procedure kits that contain non-sterile surgical patties and strips, which could lead to endotoxin contamination. This poses a risk of infection or other health issues if used in medical procedures.
The kits include non-sterile Codman Surgical Patties and Surgical Strips that can have endotoxin contamination. Endotoxins are bacterial components that can cause infections or adverse reactions when used in medical procedures.
Healthcare professionals and medical facilities that use these specific custom kits are most at risk. Patients receiving procedures with these kits may also be affected if the contamination occurs.
Check for kits labeled with specific model numbers like FREE FLAP BASIC SET-UP PK (REF DYNJ0991320J) or MVFF/FIBU #54-RF (REF DYNJ21927R). Look for lot numbers listed in the recall notice.
Look for model numbers and lot numbers listed in the recall notice to determine if your kit is affected.
The recall states that the kits contain non-sterile surgical patties and strips with potential for endotoxin contamination, so they are not safe for medical use.
Check the model numbers and lot numbers on your kit against the list provided in the recall notice.
The recall does not specify a remedy, so contact Medline directly for further instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0783-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0783-2025 from Medline. 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.
