FDAMarch 9, 2018device

Proclaim DRG Implantable Pulse Generator, Model Number 3664

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

The hazard

The firm received complaints of error messages that occurred during routine impedance checks on Proclaim DRG IPGs, model 3664. Some complaints were also associated with transient over stimulation which created discomfort for the patients.

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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Proclaim DRG Implantable Pulse Generator, Model Number 3664 — Recall Details · AllClear