Medline recalls specific medical procedure kits with catheter surface finish irregularities and connector detachment risks. Affected kits have model DYNJ0040839 and lot numbers listed. No immediate action needed but check for issues.
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 medical procedure kits that have irregular catheter surfaces and connectors that may detach prematurely. This could lead to medical complications during procedures if the kits are used without proper function.
The catheters in these kits have surface finish irregularities that could cause them to detach from the funnel during use. This might lead to medical complications if the catheter becomes dislodged during a procedure.
Healthcare professionals using Medline's medical procedure kits with the specific model number DYNJ0040839 and listed lot numbers are most at risk. Patients receiving procedures using these kits may also be affected.
Check for the model number DYNJ0040839 on the kit label. Lot numbers 25JMK709, 25FMJ661, 25CMG042, 24IME549, 24GMD004, 24CMF091, 24CME465, and 24BMH490 are also affected.
Look for the model number DYNJ0040839 and the listed lot numbers on the kit packaging.
Medline identified that some kits have catheter surface finish irregularities and connectors that may detach prematurely, which could lead to medical complications.
No immediate action is required, but you should check the kit label for the model number and lot numbers to confirm if it's affected.
The recall record 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-2492-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2492-2026 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.
