Medline recalls two convenience kits with plastic syringes that may leak or break, posing health risks. Affected kits have specific pack and lot numbers. Consumers should check their kits and contact Medline for details.
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 medical convenience kits that contain plastic syringes prone to leaking or breaking. This could pose a health risk to patients using these kits.
The plastic syringes in these kits may leak or break due to quality issues. This could lead to contamination or injury if the kits are used for medical purposes.
Healthcare workers and patients using the recalled Medline convenience kits are most at risk. The kits are designed for medical use, so anyone handling them could be affected.
Check for kits labeled 'OR CLEAN UP KIT' with pack number DYK1002355X3 or 'CLEANING & CUTTING' with pack number DYNJ84657. The lot numbers are 21JFA080 for DYK1002355X3 and 23GBD229 for DYNJ84657.
Look for the specific pack numbers and lot numbers listed in the recall notice to confirm if your kit is affected.
The recall states that the kits may leak or break, posing a health risk. They are not safe to use as they are affected by quality issues.
The recall record does not mention a replacement option. Consumers should contact Medline directly for further assistance.
The recall record does not specify a remedy. Check with Medline for instructions on what to do with the affected kits.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-3039-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-3039-2024 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.
