FDAJuly 11, 2022device

NeuRx Diaphragm Pacing System (NeuRx DPS) External Pulse Generator (EPG), Part No. 23-0021.

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

The hazard

Due to a defect identified on the EPG controller printed circuit board assembly, device performance may degrade over time. Depending on the failure mode, potential adverse events include pain, muscle fatigue and decreased breathing effectiveness, arrhythmia or cardiac arrest, or the device may stop unexpectedly.

What to do

FDA enforcement status: Terminated

Brands named

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UPCs

00852184003212

Recall history

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

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