Nokia BPM+ Wireless Blood Pressure Monitor Product recall
Nokia BPM+ Wireless Blood Pressure Monitor Product System, measurement, blood-pressure, non-invasive
Why was Nokia BPM+ Wireless Blood Pressure Monitor Product recalled?
Device could not meet the requirements for systolic pressure
What should I do if I have this product?
Review the official FDA enforcement record for current 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?
7024260310
- Product
- Nokia BPM+ Wireless Blood Pressure Monitor Product System, measurement, blood-pressure, non-invasive
- Recalling firm
- Withings Sas
- Quantity
- Total 44,000 units (15,139 US/ 28,861 OUS)
- Distribution
- US Nationwide Distribution
- Recall date
- August 22, 2018
- Classification
- Class II
- Status
- Completed
- Agency
- FDA (device)