PlainRecalls
FDA Devices Moderate Class II Ongoing

MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT, REF MDS1001

Reported: October 16, 2024 Initiated: August 30, 2024 #Z-0032-2025

Product Description

MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT, REF MDS1001

Reason for Recall

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.

Details

Units Affected
52,521 units
Distribution
Worldwide distribution - US Nationwide and the countries of Panama and Jamaica.
Location
Northfield, IL

Frequently Asked Questions

What product was recalled?
MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT, REF MDS1001. Recalled by MEDLINE INDUSTRIES, LP - Northfield. Units affected: 52,521 units.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on October 16, 2024. Severity: Moderate. Recall number: Z-0032-2025.