Medline recalls automatic digital blood pressure units with faulty microchips that may not power on, show display issues, or overheat. Affected models include MDS1001U 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 automatic digital blood pressure units with a faulty microchip that may not power on, show display problems, or overheat. This could lead to inaccurate readings or potential safety risks if the unit becomes too hot.
The faulty microchip can cause the unit to fail to power on, display errors, or overheat, making it warm to the touch. This may result in inaccurate blood pressure readings or potential burns if the unit becomes too hot.
People who own or use Medline blood pressure monitors with the MDS1001U model and specific lot numbers are affected. Those who rely on these devices for regular health monitoring are most at risk.
Check for the model MDS1001U with lot numbers L230480007, L230880007, L231080007, L231280007, or L240380007. The unit has a GTIN of 00888277704049.
Ensure the blood pressure monitor powers on and displays correctly without overheating.
The faulty microchip can cause the unit to fail to power on, show display issues, or overheat, leading to inaccurate readings or potential safety risks.
The affected model is MDS1001U with lot numbers L230480007, L230880007, L231080007, L231280007, and L240380007.
Check for the model MDS1001U with 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-0033-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0033-2025 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.
