Medline recalls Centurion procedure kits with specific pack numbers due to potential leaks and breakage in 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 Centurion procedure kits labeled as 'Umbilical Vessel Tray' with pack numbers UVT1100. These kits contain plastic syringes that may leak or break, posing a risk to patient health during medical procedures.
The plastic syringes in these kits may leak or break, potentially causing contamination or injury to patients during medical procedures. This risk is linked to the FDA Safety Alert from March 19, 2024.
Healthcare professionals using these kits during medical procedures are most at risk. Patients receiving care with these kits could be affected if the syringes leak or break.
Check for Centurion procedure kits labeled 'Umbilical Vessel Tray' with pack numbers UVT1100 and specific lot numbers: 2021032280, 2021072680, 2021092780, or 2022011080.
Look for the product label indicating 'Umbilical Vessel Tray' and pack number UVT1100 with the listed lot numbers.
The plastic syringes in these kits may leak or break, potentially causing contamination or injury to patients during medical procedures.
Lot numbers 2021032280, 2021072680, 2021092780, and 2022011080.
The recall does not specify a stop-use instruction, so you can continue using them but should check for leaks or breakage.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-2769-2024 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-2769-2024 from Medline Industries. 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.
