Medline recalls custom medical procedure kits with non-sterile surgical components that may contain endotoxins. Affected kits include OPEN HEART CDS-LF and NEURO PACK models. Consumers should check product labels for lot numbers and serial codes.
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 components, which could lead to endotoxin contamination. This poses a risk of infection or complications for patients during 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 using the recalled kits are most at risk. Patients undergoing procedures with these kits could face infection or complications.
Check for labels with model numbers: OPEN HEART CDS-LF (REFCDS840451M), NEURO PACK (REFDYNJ41516M), or other listed kits. Look for lot numbers like 24BLA736, 19JKB417, or 23GBO400 on the packaging.
Look for model numbers and lot numbers on the kit packaging to confirm if it is affected.
Reach out to Medline directly to verify if your specific kit is part of the recall and get instructions for next steps.
The recall includes custom medical procedure kits labeled as OPEN HEART CDS-LF (REFCDS840451M), NEURO PACK (REFDYNJ41516M), RFD- AAA PACK (REFDYNJ54242B), OPEN HEART A&B (REFDYNJ901203C/D), ACDF-LF (REFDYNJ906681B/C).
Check for model numbers and lot numbers on the packaging. Affected kits have specific lot numbers like 24BLA736, 19JKB417, or 23GBO400.
The kits contain non-sterile surgical components that may have endotoxins, which can cause infections or complications during medical procedures.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0778-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0778-2025 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.
