Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
PiezoWave 2 Control Unit Recalled by Richard Wolf GmbH Due to The high voltage capacitor may fail early in...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Richard Wolf GmbH directly.
Affected Products
PiezoWave 2 Control Unit, Product Number 100506US, compact myofascial acoustic compression therapy device that enables treatment with piezoelectric shockwaves (Therapeutic massager).
Quantity: 31 units
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed to 1 state: GA
About Richard Wolf GmbH
Richard Wolf GmbH has 10 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report