Medline DYNJ33603F, DYNJ0547084O, DYNJ0547084P, DYNJ80875C, DYNJ80875D, DYNJ80875J, DYNJ80875K, DYNJ908306, DYNJ908306A, DYNJ64305D, DYNJ87941, DYNJ87941A, DYNJ906872B, DYNJ59614 - Product listings with UDI/DI, case UDI/DI, and lot numbers for medical devices.
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 DYNJ33603F, DYNJ0547084O, DYNJ0547084P, DYNJ80875C, DYNJ80875D, DYNJ80875J, DYNJ80875K, DYNJ908306, DYNJ908306A, DYNJ64305D, DYNJ87941, DYNJ87941A, DYNJ906872B, DYNJ59614 - Product listings with UDI/DI, case UDI/DI, and lot numbers for medical devices.
Low risk - These are standard medical device SKUs with UDI/DI and lot numbers for tracking purposes. No immediate safety concerns.
All medical device users
Check for proper UDI/DI and lot numbers to ensure product traceability and compliance with medical device regulations.
Verify the UDI/DI and lot numbers match the product specifications for the specific medical device.
Ensure the lot numbers are within the valid period for the device's intended use.
Confirm the product is registered with the appropriate regulatory body (e.g., FDA) for the intended use.
UDI/DI (Unique Device Identifier/Device Identifier) is a unique code assigned to medical devices for traceability and regulatory purposes. It helps track devices throughout the supply chain.
Ensure the product has a valid UDI/DI and lot number that matches the manufacturer's specifications. Check with the regulatory body (e.g., FDA) for approved products.
UDI (Unique Device Identifier) is a higher-level code that includes the DI (Device Identifier). The DI is the specific identifier for the device model, while the UDI is the full unique identifier for the device.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2505-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2505-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
