Medline recalls red rubber latex urethral catheter trays due to potential catheter detachment during use. Affected units include specific model numbers and lots. Consumers should 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 red rubber latex urethral catheterization trays and bags because some have issues with the catheter connector detaching from the funnel. This could lead to complications during medical procedures if the catheter becomes dislodged.
The catheter connector can detach prematurely from the catheter funnel during use. This may cause the catheter to become dislodged, potentially leading to complications in medical procedures. The issue is identified through irregularities in the catheter surface finish and dimensions.
Healthcare professionals using the catheter trays for medical procedures are most at risk. Patients receiving catheter care may also be affected if the device malfunctions.
Check for the Medline Product Number/SKU (REF) DYND10407 or UDI/DI numbers 10080196990740 (each) and 10080196990741 (case). All lots of this specific red rubber latex catheter tray and bag are affected.
Reach out to Medline directly for specific instructions on how to handle the recalled item.
The recall indicates potential issues with the catheter connector detaching, so it is not recommended to use the product until Medline provides further guidance.
Contact Medline directly for specific instructions on how to handle the recalled item.
Check for the Medline Product Number/SKU (REF) DYND10407 or UDI/DI numbers 10080196990740 (each) and 10080196990741 (case). All lots of this specific red rubber latex catheter tray and bag are affected.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2481-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2481-2026 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.
