Medline recalls laparoscopy procedure kits with irregular catheter surfaces and connector detachment risks. Affected kits have specific model numbers and lot codes.
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 laparoscopy procedure kits that have issues with catheter surfaces and connectors. These problems could lead to improper use during medical procedures.
The catheters may have irregular surfaces, connectors can detach prematurely, and the outer diameter might not meet specifications. These issues could affect proper medical procedure use.
Medical professionals using the recalled laparoscopy kits are most at risk. The recall affects specific model numbers sold through Medline.
Check for the model number DYNJ37378A on the kit. The lot numbers are listed as DYNJ37378A. The kits are labeled as 'LAPAROSCOPY COMBINED - NO NDL'.
Look for the model number DYNJ37378A on the kit label.
Medline identified issues with catheter surface finish, connector detachment, and outer diameter specifications during internal reviews.
The recall record does not specify a remedy, so no action is required beyond checking if the kit matches the description.
The recall notes potential issues with catheter performance but does not state specific safety risks like injury or death.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2485-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2485-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
