Medline recalls custom medical procedure kits with non-sterile Codman Surgical Patties & Strips that may contain endotoxins. Affected kits have specific model numbers and lot numbers listed in the recall notice.
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 Codman Surgical Patties and Strips, which could lead to endotoxin contamination. This poses a risk of infection or other health issues for patients during medical procedures.
The kits contain non-sterile Codman Surgical Patties and Strips that may have endotoxins. Endotoxins are bacterial components that can cause infections or adverse reactions when introduced into the body during medical procedures.
Healthcare professionals and medical facilities that use these specific custom kits are most at risk. Patients receiving procedures using these kits could be exposed to endotoxins.
Check for kit labels with model numbers like MEM MAXILLOFACIAL PACK-LF (REF DYNJ0660040R) or FREE FLAP PACK-LF (REF DYNJ42833A). Lot numbers listed in the recall include sequences like 19BKB772 through 24LBU103.
Look for model numbers and lot numbers on the kit packaging as listed in the recall notice.
The recall is due to the presence of non-sterile Codman Surgical Patties and Strips that may contain endotoxins, which can cause infections during medical procedures.
Kits labeled with model numbers like MEM MAXILLOFACIAL PACK-LF (REF DYNJ0660040R) or FREE FLAP PACK-LF (REF DYNJ42833A) with specific lot numbers listed in the recall notice.
Check the kit label for the model number and lot number, which are provided in the recall notice for affected kits.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0786-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0786-2025 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
