Medline recalls convenience kits with plastic syringes that may leak or break, posing health risks. Affected kits include specific model numbers and pack 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 convenience kits that contain plastic syringes which may leak or break, potentially harming patients. These kits are labeled with specific model numbers and pack numbers. Owners should check their kits against the listed identifiers to determine if they are affected.
The plastic syringes in these kits have been identified as leaking or breaking due to quality issues, which could lead to patient health risks. This is linked to a recent FDA safety alert from March 19, 2024.
Healthcare workers and patients using Medline convenience kits with the listed model numbers and pack numbers are most at risk. The recall targets specific kits sold in the U.S. market.
Check for model numbers DYNJ39451D, DYNJ59573A, or DYNJ80281A with the listed pack numbers or lot numbers on the kit's label.
Look for model numbers and pack numbers on the kit's label to see if they match the recalled items.
The recall indicates potential leaks or breakage, so affected kits should not be used until the issue is resolved.
Check the kit's label for the model numbers and pack numbers listed in the recall to determine if it is affected.
Compare your kit's model number and pack number with the specific identifiers listed in the recall notice.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2985-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2985-2024 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.
