Medline recalls Centurion procedure packs with specific pack numbers due to potential leaks and breakage of plastic syringes that could harm patients during medical procedures.
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
Medline is recalling several Centurion procedure packs that include plastic syringes which may leak or break, posing a risk to patient health. This recall is important because medical procedures using these kits could be affected by the quality issues.
The plastic syringes in these procedure packs can leak or break, potentially causing harm to patients during medical procedures. This risk is related to the quality issues identified in the syringes, which may not be severe enough to cause serious injury in normal use.
Healthcare providers using the recalled Centurion procedure packs are most at risk, particularly those performing procedures involving the syringes. Patients receiving care with these kits may also be affected.
Check for Centurion procedure packs labeled as BIOPSY TRAY-LF (Pack Number SPEC4380), CIRCUMCISION TRAY (Pack Number CIT6325), or other specific models listed in the recall notice.
Look for the specific pack numbers listed in the recall notice to identify affected Centurion procedure packs.
Medline is recalling Centurion procedure packs that contain plastic syringes which may leak or break, posing a risk to patient health.
Check for the specific pack numbers listed in the recall notice, such as SPEC4380 for BIOPSY TRAY-LF or CIT6325 for CIRCUMCISION TRAY.
The recall notice does not specify a remedy, so you should check with 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-2773-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2773-2024 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.
