Medline recalls certain Automatic Digital Blood Pressure Monitors due to faulty microchips causing overheating and display failures. Check lot numbers inside.
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.
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Contact the company
📍Recalling firmMEDLINE INDUSTRIES, LP - Northfield3 Lakes Dr · Northfield, IL 60093-2753
✎ GovInfoNow plain-language explainer
Medline Industries is recalling the Automatic Digital Blood Pressure Monitor (REF MDS1001UT) because a faulty microchip can cause the device to overheat or fail to power on. The unit may become warm to the touch during use, and the display screen may show issues after only a few uses. This affects 7,428 units distributed in the US, Panama, and Jamaica. Read more at govinfonow.com/recall/54135-medline-blood-pressure-monitor-mds1001ut-faulty-microchip-causes-power-issues.
“Medline Blood Pressure Monitor Recall: Overheating & Display Issues.” GovInfoNow, updated October 13, 2026. https://govinfonow.com/recall/54135-medline-blood-pressure-monitor-mds1001ut-faulty-microchip-causes-power-issues. Based on FDA recall #Z-0034-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0034-2025%22&limit=1).
The FDA announced on Aug. 30, 2024, that Medline Industries LP is recalling Automatic Digital Blood Pressure Monitors due to overheating and display issues. The recall affects units distributed in the U.S., Panama, and Jamaica.
How to tell if you have it
MEDLINE Automatic Digital Blood Pressure Monitor, REF MDS1001UT
UPC 00193489012548
Lot Numbers: L230480008, L230780008, L231080008, L231280008, L240280008
The hazard
Certain monitors with a faulty microchip may fail to power on or show display screen issues after initial use. The units may also overheat and become warm to the touch.
Context
GovInfoNow's records show Medline Industries LP has issued 119 other recalls since Oct. 22, 2021. Recent examples include a July 25, 2025 recall for light failure in newborn resuscitation kits and a July 23, 2025 recall for Foley Tray Kits with incorrect labeling. Other recent recalls of similar products include BD Pyxis MedStation ES Tower 352 Medication Cabinet Recall (April 30, 2026), BD Pyxis MedStation ES REF 323 Medication Cabinet Recall (April 30, 2026), and BD Pyxis MedBank Mini 1147-00 Medication Cabinet Recall (April 30, 2026).
How to tell if you have this one
Check if your device is a Medline Automatic Digital Blood Pressure Monitor with REF MDS1001UT. Look for one of these lot numbers on the packaging or device: L230480008, L230780008, L231080008, L231280008, or L240280008. The GTIN is 00193489012548.
Brand
Medline
Product
MEDLINE Automatic Digital Blood Pressure Monitor, REF MDS1001UT
Category
Medical device
FDA recall event · 3 products
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Ongoing
Distribution
Worldwide distribution - US Nationwide and the countries of Panama and Jamaica.
Recall number
Product, codes & lots
Quantity
Z-0032-2025
MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT, REF MDS1001; GTIN 00888277629656, Lot Numbers: L230380005, L230480005, L230580005, L230680005, L230780005, L230980005, L231080005, L231180005, L231280005, L240280005
52,521 units
Z-0033-2025
MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT, REF MDS1001U.; GTIN 00888277704049. Lot Numbers: L230480007, L230880007, L231080007, L231280007, L240380007
9.608 units
Z-0034-2025
MEDLINE Automatic Digital Blood Pressure Monitor, REF MDS1001UT.; GTIN 00193489012548 Lot Numbers: L230480008, L230780008, L231080008, L231280008, L240280008
7,428 units
Based on the official FDA remedy
What to do — step by step
Check Your Device
Verify if your blood pressure monitor matches the recalled REF MDS1001UT and has one of the affected lot numbers.
Monitor for Overheating
If you continue to use the device, watch for it becoming warm to the touch or displaying screen issues after a few uses.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
Nationwide
Not listed
FDA distribution: “Worldwide distribution - US Nationwide and the countries of Panama and Jamaica.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA published this recall 47 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #Z-0034-2025 (August 30, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0034-2025 to see it in context.
Plain-language summary written by qwen3.6:35b-a3b on October 13, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.