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.
- CPSCWolf Appliance Recalls Dual Fuel Ranges with Infrared Griddles Due to Burn and Fire Hazards2024-11-07
- FDAHenke-Ject-2 part luer sterile single use syringes - used for intravenous, intramuscular, subcutaneous, intracutaneous and intraarterial injection of liquids or diluted drugs in combination with an adequate medical device or for withdrawal of fluids from the body. Ref: 4100.000V02023-07-27
- FDAFLEX. GRASP. FORCEPS 6.6FR WL 550MM, Product Number 8736.6852023-03-24
- FDAFLEX. GRASP. FORCEPS 5FR WL 550MM, Product Number 8735.6852023-03-24
- FDAFLEX. GRASP. FORCEPS 5FR WL 550MM, Product Number 828.0512023-03-24
- FDAFLEX. BIOPSY FORCEPS 5FR WL 550MM, Product Number 829.0512023-03-24
- FDALake Wolf Creamery Queso Fresco, crumbling fresh cheese, refrigerated, vacuum packaged in flexible plastic packages, net wt. 1.5 lbs. or 0.5 lbs. No UPC.2021-09-30
- FDALake Wolf Creamery Cheddar Curds, cheese curds, refrigerated, packaged in container with sealed lidded cups. net wt. 0.5 lbs. No UPC.2021-09-30
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