Medline recalls Centurion medical procedure kits that may contain non-sterile products if the breather pouch seal is opened. Affected kits have specific lot numbers and labels for umbilical cut down and plastics suture trays.
It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.
Medline is recalling Centurion medical procedure kits that could lead to using non-sterile products if the breather pouch seal is opened. This is a risk for healthcare workers using these kits during medical procedures.
The breather pouch seal may open unintentionally, allowing non-sterile products to be used. This could lead to infections or complications for patients during medical procedures.
Healthcare workers using the Centurion kits for medical procedures are most at risk. Patients receiving care from these kits could be affected if non-sterile products are used.
Check for labels with 'FLOOR - UMBILICAL CUT DOWN TRA' or 'PLASTICS SUTURE TRAY'. Look for lot numbers 23LBO858 or 23LBL653 on the packaging.
Inspect the breather pouch seal to ensure it is intact and not opened.
The kits may contain non-sterile products if the breather pouch seal is opened, so they should be checked for seal integrity before use.
Lot numbers 23LBO858 and 23LBL653 are affected.
Look for labels indicating 'FLOOR - UMBILICAL CUT DOWN TRA' or 'PLASTICS SUTURE TRAY' with the specific lot numbers.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0150-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0150-2025 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.
