Medline recalls custom medical procedure kits with non-sterile surgical components that may contain endotoxins. Affected kits include specific models and lot numbers. Consumers should check their kits for the listed references and lot numbers.
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 materials which could have 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 may contain 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 Medline custom kits are most at risk. Patients receiving procedures with these kits could be exposed to potential contamination.
Check for kits labeled as PANENDOSCOPY-LF (REF DYNJ36728C) or ENDOSCOPIC SINUS PACK (REF DYNJ40644A or DYNJ66449). Look for specific lot numbers listed in the recall notice.
Look for the product references and lot numbers listed in the recall notice to confirm if your kit is affected.
The kits contain non-sterile Codman Surgical Patties and Surgical Strips that have the potential for endotoxin contamination.
The recall notice does not specify a remedy, so check the product labels and lot numbers to determine if your kit is affected.
Yes, the recall lists specific lot numbers for each product reference that you can check against.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0785-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0785-2025 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.
