FDASeptember 12, 2017device

Proclaim DRG Implantable Pulse Generator Model 3664

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

The hazard

Analysis of the difference between the actual device longevity and the battery indicator status provided by the Clinician Programmer (CP) or Patient Controller (PC) has revealed errors in the CP or PC longevity estimations that can overestimate or under estimate the battery indicator status in certain situations.

What to do

FDA enforcement status: Terminated

Brands named

st jude medical

Recall history

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

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