Medline recalls 40+ medical convenience kits with plastic syringes that may leak or break, posing health risks. Affected kits have specific pack numbers and lot numbers listed in the recall.
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 40 different medical convenience kits that contain plastic syringes which may leak or break, potentially causing health risks. These kits were sold with specific pack numbers and lot numbers listed in the recall.
The plastic syringes in these kits have been identified as leaking or breaking, which could pose a risk to patient health. This issue is related to the FDA Safety Alert issued on March 19, 2024.
Healthcare professionals and medical facilities that use these kits are most at risk. Patients using the kits may be affected if the syringes leak or break.
Check for specific pack numbers and lot numbers listed in the recall, such as DYKMBNDL200A, DYNDL1495A, and others. The kits are labeled as 'Medline Convenience kits' with the listed pack numbers.
Look for specific pack numbers and lot numbers listed in the recall to determine if your kit is affected.
The plastic syringes in these kits may leak or break, posing a risk to patient health, as identified by the FDA Safety Alert on March 19, 2024.
Check for specific pack numbers and lot numbers listed in the recall, such as DYKMBNDL200A, DYNDL1495A, and others.
The recall does not specify a remedy, so contact Medline directly for further instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-3028-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-3028-2024 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.
