Medline recalls specific ARTHROGRAM TRAY and TOL NEURO ANGIO PACK models due to rescinded 510(k) regulatory clearances for medical devices. Affected units include model numbers DYNJ07425 and DYNJ38610I.
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Medline is recalling certain ARTHROGRAM TRAY and TOL NEURO ANGIO PACK medical kits because their 510(k) regulatory clearances have been rescinded. This means the devices may not meet safety standards and could pose risks during medical procedures.
The 510(k) regulatory clearances for certain medical devices have been rescinded, meaning the devices may not meet safety standards. This could lead to potential risks during medical procedures if the devices are used without proper regulatory approval.
Healthcare professionals using these specific medical kits in hospitals or clinics are most at risk. Patients receiving procedures with these kits could be affected if the devices are used without proper regulatory approval.
Check for model numbers DYNJ07425 (ARTHROGRAM TRAY) or DYNJ38610I (TOL NEURO ANGIO PACK) on the product. Lot numbers 23DBP927, 23EBS362, 25DBM593, 25GBO740, and others are also affected.
Identify the model number and lot number on the product 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The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded, meaning the devices may not meet safety standards.
Check the model number and lot number on the product to confirm if it is affected. If it is, contact Medline for further instructions.
The recall is due to rescinded regulatory clearances, but specific safety risks are not detailed in the official notice.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1844-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1844-2026 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.
