Medline recalls red rubber latex urethral catheterization trays due to potential catheter detachment during use. Affected units have specific product numbers and were sold in all lots.
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 red rubber latex urethral catheterization trays and bags that may detach from the catheter funnel during use. This could lead to injury if the catheter becomes dislodged while in the body.
The catheter may detach prematurely from the funnel during use, which could cause injury if the catheter becomes dislodged inside the body. The catheter surface finish irregularities and size issues may contribute to this problem.
Healthcare professionals using the catheter trays for medical procedures are most at risk. Patients receiving catheter care may also be affected if the device fails during use.
Check for the product number DYND18350 on the tray or bag. The item is red rubber latex and has a 15 French size. All lots were affected.
Verify the product number DYND18350 on the tray or bag to confirm it is affected.
The recall indicates potential issues with catheter detachment, so it is not recommended for use until the remedy is applied.
The recall does not specify a remedy, so contact Medline directly for guidance.
The recall mentions potential injury from dislodged catheters, but does not specify patient risks in detail.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2482-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2482-2026 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.
