Medline 983911J, 983911L, DYNJ65924D, DYNJ65924F, DYNJ900273D, DYNJ900273F, CDS984596F, CDS985201A, CDS982891F - UDI/DI & Lot Numbers
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 983911J, 983911L, DYNJ65924D, DYNJ65924F, DYNJ900273D, DYNJ900273F, CDS984596F, CDS985201A, CDS982891F - UDI/DI & Lot Numbers
Low risk - These are Medline product UDI/DI and Lot Numbers for medical devices. No immediate danger.
Healthcare Professionals
Check UDI/DI and Lot Numbers for each product to ensure they match the expected specifications for your medical device.
Verify the UDI/DI and Lot Numbers for each product to ensure they match the expected specifications for your medical device.
Ensure that the UDI/DI and Lot Numbers are within the valid range for the product and lot number.
Contact Medline customer support for further assistance if you have any concerns.
UDI/DI (Unique Device Identification/Device Identifier) is a unique code assigned to medical devices to track them. Lot Numbers are used to identify the batch of a product.
Check the UDI/DI and Lot Numbers against the product specifications and the manufacturer's documentation to ensure they match.
Contact Medline customer support for further assistance or report the issue to the appropriate regulatory body.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2506-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2506-2026 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.
