Richard Wolf recalls

2 official recalls and safety alerts involving Richard Wolf since 2023-05, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.

This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Richard Wolf or the relevant agency.

1. 2025-05-21
2. US
   Drugs & medicalClass II

   Richard Wolf GmbH recalls PiezoWave 2 Control Unit, Product Number 100506US, compact myofascial acoustic compression therapy device that enables treatment with…

   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…

   FDA · DeviceRichard Wolf GmbHUS State: GAOfficial notice →
3. 2023-05-03
4. US
   Drugs & medicalClass II

   Richard Wolf GmbH recalls FLEX. BIOPSY FORCEPS 5FR WL 550MM, Product Number 829.051

   Potentially unable to open forceps jaws when the endoscope shaft is bent by about 90 degrees. If, in addition, the proximal forceps shaft is bent, the forceps can no longer be opened or restrictions begin even with a…

   FDA · DeviceRichard Wolf GmbHWorldwide distribution - US Nationwide and the countries of United Arab…Official notice →