Medline recalls red rubber latex urethral catheterization trays with irregular surface finishes and connector detachment risks. Affected models include DYNC1816 and DYND10350, 15 Fr. sizes. Stop using immediately to avoid potential injury.
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 ureth:thral catheterization trays that have surface irregularities and may detach prematurely. This could lead to injury during medical procedures if the catheter disconnects from the funnel.
The catheter surface finish irregularities can cause the connector to detach from the catheter funnel during use. This detachment risk could lead to injury if the catheter becomes dislodged during medical procedures.
Healthcare professionals using these catheter trays for medical procedures are most at risk. Patients receiving catheter care may also be affected if the tray is used improperly.
Check for red rubber latex trays with model numbers DYNC1816 or DYND10350, 15 Fr. sizes. The product includes specific UDI/DI numbers listed in the recall notice.
Discard the recalled catheter trays to prevent potential detachment during medical procedures.
The affected models are DYNC1816 and DYND10350, 15 Fr. sizes with specific UDI/DI numbers listed in the recall notice.
Medline identified that some samples had surface finish irregularities and connector detachment issues that could lead to injury during medical procedures.
Check for red rubber latex trays with model numbers DYNC1816 or DYND10350, 15 Fr. sizes and the specific UDI/DI numbers listed in the recall notice.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2480-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2480-2026 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.
