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Richard Wolf GmbH recalls PiezoWave 2 Control Unit, Product Number 100506US, compact myofascial acoustic compression therapy device that enables t
Recalled May 21, 2025 · FDA recall Z-1753-2025 · Richard Wolf
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. · FDA Class II
Units
31 units
Sold at
US State: GA
Description
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.
Product
PiezoWave 2 Control Unit, Product Number 100506US, compact myofascial acoustic compression therapy device that enables treatment with piezoelectric shockwaves (Therapeutic massager).
Manufacturer(s)
Richard Wolf GmbH
Made in
Germany
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →