Medline recalls specific Centurion procedure kits due to potential leaks and breakage in plastic syringes, which may pose health risks 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 certain Centurion procedure kits that contain plastic syringes prone to leaks and breakage. This could lead to patient health risks if used in medical procedures.
The plastic syringes in these kits may leak or break, potentially causing patient health issues during medical procedures. This risk is linked to the FDA Safety Alert from March 19, 2024.
Healthcare providers using the recalled Centurion procedure kits are most at risk, particularly those handling the kits in medical settings.
Check for kits labeled as BIOPSY KIT (Pack Number DYNDA1466A), BIOPSY SKIN/LACERATION TRAY (Pack Number SUT20455), or other specified Centurion trays with the listed lot numbers.
Look for the product names and pack numbers listed in the recall notice to confirm if your kit is affected.
The recall is due to potential leaks and breakage in plastic syringes, which could pose health risks during medical procedures as noted in the FDA Safety Alert from March 19, 2024.
The recalled products include BIOPSY KIT (Pack Number DYNDA1466A), BIOPSY SKIN/LACERATION TRAY (Pack Number SUT20455), and other Centurion procedure kits with specific lot numbers listed in the recall notice.
The recall does not require immediate stop use; however, healthcare providers should check the product labels to confirm if their kits are affected.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2766-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2766-2024 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.
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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.
