MEDLINE recalls automatic digital blood pressure monitors with faulty microchips that may fail to power on or overheat. Affected models include REF MDS1001UT with specific lot numbers.
It has been determined that certain Blood Pressure Monitors containing a faulty microchip have failed to power on or have shown display screen issues after the initial few uses, as well as overheating at times making the unit warm to the touch.
MEDLINE is recalling blood pressure monitors with a faulty microchip that may not power on or overheat. This could lead to inaccurate readings or safety risks if the device becomes too hot to handle.
The faulty microchip causes the device to sometimes fail to power on or show display issues after initial use. It can also overheat, making the unit warm to the touch, which may lead to inaccurate readings or potential burns if handled while hot.
Owners of MEDLINE Automatic Digital Blood Pressure Monitors with model REF MDS1001UT and specific lot numbers are affected. People who rely on this device for regular blood pressure monitoring are most at risk.
Check for the model REF MDS1001UT on the device. The lot numbers L230480008, L230780008, L231080008, L231280008, and L240280008 are affected. These units were sold with specific GTIN 00193489012548.
Ensure the monitor powers on and displays correctly without overheating.
The faulty microchip causes the device to sometimes fail to power on or show display issues after initial use, and it can overheat making the unit warm to the touch.
The affected model is REF MDS1001UT with lot numbers L230480008, L230780008, L231080008, L231280008, and L240280008.
Check for the model REF MDS1001UT and the specific lot numbers listed in the recall notice.
We’ve drafted a message you can send MEDLINE to request your refund or repair — edit it as you like.
Subject: Recall Z-0034-2025 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-0034-2025 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.
