Medline recalls 40+ Centurion procedure kits with plastic syringes that may leak or break, posing health risks. Check pack numbers and lot dates for affected items.
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 40 different procedure kits that contain plastic syringes with potential leaks or breakage. This could pose a risk to patient health during medical procedures.
The plastic syringes in these kits have been identified by the FDA as having leaks or breakage issues. This could lead to potential contamination or injury during medical procedures.
Healthcare providers and medical facilities using these kits are likely affected. Patients using these kits during procedures may be at risk if the syringes leak or break.
Check for the product names listed in the recall (e.g., ARTHROGRAM TRAY) and the specific pack numbers and lot dates provided in the record.
Identify the product name and pack number from the list provided in the recall notice.
The recall states that these kits contain plastic syringes that may leak or break, posing a risk to patient health. They are not safe to use as described.
Check the product name and pack number against the list provided in the recall notice. Affected kits include specific items like ARTHROGRAM TRAY with pack numbers DYNDH1349, SPEC0400, etc.
The recall does not specify a remedy, so no action is required beyond checking if you have an affected kit.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2772-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2772-2024 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.