FDAAugust 28, 2017device

Anthem Model Numbers: PM3210, PM3212; Allure/Relieve Model Numbers: PM3222, PM3242, PM3262, PM3542, PM3224, PM3244 Implantation of a single-chamber pulse generator, dual-chamber pulse generator, or CRT-P is indicated in one or more of the following permanent conditions: Syncope, Presyncope, Fatig...

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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