FDAJune 11, 2018device

Nokia BPM+ Wireless Blood Pressure Monitor Product System, measurement, blood-pressure, non-invasive

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Device could not meet the requirements for systolic pressure

What to do

FDA enforcement status: Completed

Brands named

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Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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