Richard Wolf GmbH: Device Recall
Recall #Z-1753-2025 · 04/09/2025
Class II: Risk
Recall Details
- Recall Number
- Z-1753-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Richard Wolf GmbH
- Status
- Ongoing
- Date Initiated
- 04/09/2025
- Location
- Knittlingen, Germany
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 31 units
Reason for Recall
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 Description
PiezoWave 2 Control Unit, Product Number 100506US, compact myofascial acoustic compression therapy device that enables treatment with piezoelectric shockwaves (Therapeutic massager).
Distribution Pattern
US State: GA
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.