Medline Blood Pressure Unit (Medline) – Microchip Failure (2024)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT, REF MDS1001
Brand
MEDLINE INDUSTRIES, LP Northfield
Lot Codes / Batch Numbers
GTIN 00888277629656, Lot Numbers: L230380005, L230480005, L230580005, L230680005, L230780005, L230980005, L231080005, L231180005, L231280005, L240280005
Products Sold
GTIN 00888277629656, Lot Numbers: L230380005, L230480005, L230580005, L230680005, L230780005, L230980005, L231080005, L231180005, L231280005, L240280005
MEDLINE INDUSTRIES, LP Northfield is recalling MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT, REF MDS1001 due to It has been determined that certain Blood Pressure Monitors containing a faulty microchip have failed to power on or have shown display screen issues . Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
Medline issued a MEDICAL DEVICE RECALL notice to its consignees on 08/30/2024 via email and USPS first class mail. The notice explained the problem, risk to user and requested that units demonstrating the failure be discarded. If you have any questions, contact the Recall Department at 866-359-1704 or recalls@medline.com. Medline issued a follow up notification to distributors on 09/13/2024. The notification contained the same information as the initial letter, but also instructed distributors to notify customers if the product was further distributed.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026