Medline recalls specific chest tube convenience kits due to leaks and breakage risks. Affected kits include models with pack numbers CHT2120 and DYNDA2475. Learn how to identify and safely handle recalled items.
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 several chest tube convenience kits that may leak or break, posing a risk to patient health. These kits could cause harm if used improperly or if they fail during medical procedures.
The kits contain plastic syringes that may leak or break, potentially causing patient health issues. This risk is linked to quality problems identified by the FDA in March 2024.
Healthcare professionals and patients using these kits for chest tube procedures are most at risk. The recall affects specific models sold in the U.S. market.
Check for pack numbers listed in the recall: CHT2120, DYNDA2475, DYNDA2941A, DYNDA2998, DYNDH1794, DYNJ04474F, DYNJ66222B, DYNJ67988A, DYNJ83950, DYNJ85264, DYNJ904606C, and MNS15250. Also look for specific lot numbers associated with each pack number.
Look for pack numbers and lot numbers listed in the recall notice to confirm if your kit is affected.
The recall indicates potential leaks and breakage risks, so affected kits should not be used until replaced with a safe alternative.
Check for specific pack numbers and lot numbers listed in the recall notice, such as CHT2120 or DYNDA2475 with associated lot numbers.
The recall does not specify a remedy, so contact Medline directly to determine next steps for 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-3040-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-3040-2024 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.
