Medline recalls two procedural kits (LEEP PACK and TRAB BUCKLE DSC) due to leaks and breakage risks that could harm patients. Affected kits have specific pack numbers and lot numbers.
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 two types of procedural kits that may leak or break, posing risks to patient health. These kits were sold with specific pack numbers and lot numbers identified in the recall notice.
The kits contain plastic syringes that can leak or break, potentially causing harm to patients. This issue was identified through an FDA safety alert from March 19, 2024.
Healthcare professionals using Medline procedural kits are likely affected. Patients receiving care with these kits may be at risk if leaks or breakages occur.
Check for the LEEP PACK with pack number DYNJ40348G or the TRAB BUCKLE DSC with pack number DYNJ63036B. Lot numbers 23HBR333 and 23IDC131 are also associated with these kits.
Identify the pack number and lot number on the kit to confirm if it's affected.
The recall is due to leaks and breakage risks in the plastic syringes that could harm patients, as identified by an FDA safety alert from March 19, 2024.
The LEEP PACK with pack number DYNJ40348G and the TRAB BUCKLE DSC with pack number DYNJ63036B are affected.
Check the pack number and lot number on the kit. Affected kits have pack numbers DYNJ40348G or DYNJ63036B and lot numbers 23HBR333 or 23IDC131.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2763-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2763-2024 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.
