Medline recalls convenience kits with plastic syringes that may leak or break, posing health risks. Affected kits include specific models and pack numbers. Consumers should check their items 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 convenience kits that contain plastic syringes which may leak or break, potentially causing health risks. These kits are used in medical settings and were distributed with specific model numbers and pack numbers.
The plastic syringes in these kits may leak or break, which could lead to health issues for patients. This is due to quality issues identified by the FDA Safety Alert from March 19, 2024.
Healthcare providers and patients using medical convenience kits with plastic syringes. Those who have the specific model numbers and pack numbers listed are most at risk.
Check for kits labeled with model numbers like TRACH CDS-LF (Pack Number CDS983142B) or MER TRACH CDS (Pack Number CDS984376B). Also look for Flexible LMA Packs with Syringe and Lube in sizes 1 through 5 with specific pack numbers.
Look for model numbers and pack numbers listed in the recall notice to confirm if your kit is affected.
The recall states that these kits may leak or break, posing a health risk. Affected kits should not be used until the issue is resolved.
Check the model number and pack number on your kit against the list provided in the recall notice.
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-2982-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2982-2024 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.
