Medline Industries, LP
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 Industries, LP
Low risk
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UDI/DI: 10198459134074 (each), 40198459134075 (case), Lot Number 25CLA752
Ensure that the UDI/DI and Lot Number match the ones listed for the specific product.
If there is a discrepancy, contact Medline customer service for further assistance.
UDI/DI: 10198459134074 (each), 40198459134075 (case), Lot Number 25CLA752
Yes, this product is safe as it is from Medline Industries, LP.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2497-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2497-2026 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.
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