Medline recalls three procedure kit models with possible leaks and breakage that could affect patient health. Affected kits have specific pack numbers and lot codes.
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 three types of procedure kits that may leak or break, posing a risk to patient health. These kits were sold with specific pack numbers and lot codes identified in the recall notice.
The kits contain plastic syringes that may leak or break, which could lead to patient health risks. This issue was identified through an FDA safety alert from March 19, 2024.
Healthcare professionals using these procedure kits are most at risk. Patients receiving procedures with these kits could be affected if leaks or breakage occur.
Check for pack numbers: DYNJ62734A, DYNJ44115A, or DYNJ68393A. Lot numbers include 21IME904A, 21EMF484A, or 22KBW583A.
Look for the pack number and lot number on the kit label to confirm if it's affected.
Medline recalls three procedure kits: CT BIOPSY PACK (Pack Number DYNJ62734A), E R C P PACK (Pack Number DYNJ44115A), and LARGE BIOPSY PACK NTX (Pack Number DYNJ68393A).
The kits contain plastic syringes that may leak or break, which could pose a risk to patient health as identified by an FDA safety alert from March 19, 2024.
Check the pack number and lot number on the kit label. Affected kits have specific pack numbers: DYNJ62734A, DYNJ44115A, or DYNJ68393A, and lot numbers: 21IME904A, 21EMF484A, or 22KBW583A.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1440-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1440-2025 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.
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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.
