Medline recalls specific urology procedure kits due to catheter surface finish irregularities and connector detachment risks. Affected kits have unique SKUs and lot numbers; users should check their product 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 certain urology procedure kits because some catheters have surface finish issues and may detach from the funnel during use. This could lead to complications during medical procedures if the kit is used without proper function.
The catheters in these kits have irregular surface finishes and may detach from the funnel prematurely. This can cause the catheter to become dislodged during medical procedures, potentially leading to complications like bleeding or infection.
Healthcare professionals using the recalled Medline urology procedure kits are most at risk. Patients receiving procedures with these kits may face complications if the catheter detaches.
Check for the Medline Kit Number/SKU DYKMBNDL117C or DYNJ908978/DYNJ908978F with specific lot numbers listed in the recall notice. These kits were sold with unique UDI/DI and lot numbers.
Identify your kit's Medline SKU and lot number to confirm if it's affected. The affected kits have specific SKUs and lot numbers listed in the recall.
The recall indicates potential issues with catheter surface finish and connector detachment, so they should not be used until confirmed safe.
Check your kit's SKU and lot number against the list provided in the recall notice to determine if it's affected.
The recall does not specify a replacement process; users should 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-2495-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2495-2026 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.
