FDAAugust 28, 2017device

PM1214 NUANCE SR RF; PM1230 and PM2230 NUANCE MRI; PM2214 NUANCE DR RF These low voltage (LV) devices are implantable pacemaker pulse generators, intended to be permanently implanted in the body, that have a power supply and electronic circuits that produce a periodic electrical pulse to stimulat...

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

The hazard

New pacemaker firmware was developed to further mitigate the risk of unauthorized access to our pacemakers that utilize radio frequency (RF) communications.

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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