Medline recalls ARTHROSCOPY PACK model DYNJ82440 due to rescinded 51:0(k) regulatory clearances. 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The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.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 ARTHROSCOPY PACKs with model number DYNJ82440 because regulatory clearances for certain medical components have been rescinded.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 specific medical components like Control Syringes, Guidewires, and High-Pressure Tubing. This means the products may not have been properly tested for safety and could lead to complications during medical procedures.
Healthcare professionals using the ARTHROSCOPY PACKs with model DYNJ82440 and lot numbers 24BMD005 are most at risk. Patients receiving these products during surgery may also be affected.
Check for model number DYNJ82440 on the ARTHROSCOPY PACK. Affected units have UDI-DI codes 10195327196240 and 40195327196241, and lot number 24BMD005.
Identify the model number and lot number on the ARTHROSCOPY PACK to confirm if it is affected.
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded, meaning the products may not meet safety standards.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.
Affected products have model number DYNJ82440, UDI-DI codes 10195327196240 and 40195327196241, and lot number 24BMD005.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1850-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1850-2026 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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