Medline recalls 15 types of medical procedure kits with irregular catheter surfaces and detachment risks. Affected kits have specific SKUs and lot numbers. Consumers should check their kits and contact Medline for details.
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
Medline is recalling 15 different medical procedure kits due to issues with catheter surfaces and potential detachment. These problems could lead to improper use during medical procedures if the catheter disconnects from the funnel.
The recalled kits have catheters with irregular surface finishes that may cause detachment from the funnel during use. This could lead to improper medical procedures if the catheter disconnects mid-use.
Healthcare professionals and medical facilities using the recalled Medline procedure kits are most at risk. The issue affects specific kits with irregular catheter surfaces and detachment problems.
Check if your kit has a Medline label with one of the listed SKUs (e.g., DYNJ47625B, DYNJ912219) and the corresponding lot numbers (e.g., 21LBI584).
Look for the Medline label with the specific SKU and lot number listed in the recall notice.
The recall indicates potential detachment issues, so it's recommended to check if your kit is affected before use.
Check the kit label for the specific SKU and lot number listed in the recall notice.
Contact Medline directly for further instructions on how to handle the affected kit.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2501-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2501-2026 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.
