Reported May 21, 2025 · Ongoing
PiezoWave 2 Control Unit, Product Number 100506US, compact myofascial acoustic compression therapy device that enables…
Richard Wolf GmbH
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Richard Wolf GmbH · Pforzheimer Str. 32 · Knittlingen · N/A
Is this the product you have?
- PiezoWave 2 Control Unit, Product Number 100506US, compact myofascial acoustic compression therapy device that enables treatment with piezoelectric shockwaves (Therapeutic massager).
- Lot codes and dates
- UDI-DI00814334022863
- Serial Numbers
5000553232500055323350005532345000553235500055323650005532375000553238500055323950005532405000553241500055324250005532435000553244500055324550005532465000553247500055324850005532495000553250500055325150005534825000553483500055348450005534855000553486500055348850005535025000553503500055350450005535055000553506
- Amount recalled
- 31 units
Where it was sold
Why it was 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.
This product could cause temporary or reversible health problems — stop using it.
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