Medline Automatic Digital Blood Pressure Unit recall
MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT, REF MDS1001
Why was Medline Automatic Digital Blood Pressure Unit 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.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
GTIN 00888277629656, Lot Numbers: L230380005, L230480005, L230580005, L230680005, L230780005, L230980005, L231080005, L231180005, L231280005, L240280005
- Product
- MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT, REF MDS1001
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Quantity
- 52,521 units
- Distribution
- Worldwide distribution - US Nationwide and the countries of Panama and Jamaica.
- Recall date
- October 16, 2024
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)