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Withings Sas recalls Nokia BPM+ Wireless Blood Pressure Monitor Product System, measurement, blood-pressure, non-invasive
Recalled August 22, 2018 · FDA recall Z-2829-2018 · Withings Sas
Hazard
Device could not meet the requirements for systolic pressure · FDA Class II
Units
Total 44,000 units (15,139 US/ 28,861 OUS)
Sold at
US Nationwide Distribution
Description
Device could not meet the requirements for systolic pressure
Product
Nokia BPM+ Wireless Blood Pressure Monitor Product System, measurement, blood-pressure, non-invasive
Manufacturer(s)
Withings Sas
Made in
France
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →