Medline recalls PICC trays with model DYNJ41648A due to rescinded 510(k) regulatory clearances for related medical devices. Affected units include specific lot numbers and UDI-DI codes.
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Medline is recalling PICC trays with model number DYNJ41648A because regulatory clearances for related medical devices have been rescinded. This means the products may not meet safety standards and could pose risks during medical procedures.
The recall is triggered by the rescission of 510(k) regulatory clearances for certain control syringes, guidewires, and high-pressure tubing. This means the devices may not have been properly tested for safety before being used in medical procedures.
Healthcare professionals using Medline PICC trays with model DYNJ41648A and specific lot numbers are most at risk. Patients receiving care with these devices may also be affected.
Check for model number DYNJ41648A on the PICC tray. Look for lot numbers 25CLA242 or 24LLA758 and UDI-DI codes 10198459062834 (each) or 40198459062835 (case).
Identify the model number, lot number, and UDI-DI codes to confirm if your PICC tray is affected.
The 510(k) regulatory clearances for related medical devices have been rescinded, meaning the products may not meet safety standards.
The recall record does not specify a remedy, so check the product details to confirm if it is affected and contact Medline for further instructions.
Yes, lot numbers 25CLA242 and 24LLA758 are affected.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1837-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1837-2026 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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