FDAApril 9, 2025device

PiezoWave 2 Control Unit, Product Number 100506US, compact myofascial acoustic compression therapy device that enables treatment with piezoelectric shockwaves (Therapeutic massager).

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

The hazard

The high voltage capacitor may fail early in the product life cycle after delivery of surge voltages. When this failure occurs, the capacitor may produce smoke and a burning smell. In extremely rare instances a capacitor may cause a spark or excessive heat when an internal capacitor failure occurs.

What to do

FDA enforcement status: Ongoing

Brands named

richard wolfrichard

UPCs

00814334022863

Recall history

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

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