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Richard Wolf GmbH FDA Recalls
6 recalls on file across devices, 0 of them Class I and 5 still open. This firm is not matched to a listed company.
Newest first
Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.
| Product |
|---|
| PiezoWave 2 Control Unit, Product Number 100506US, compact myofascial acoustic compression therapy device that enables tClass IIApr 9, 2025The high voltage capacitor may fail early in the product lif |
| FLEX. GRASP. FORCEPS 5FR WL 550MM, Product Number 8735.685Class IIMar 24, 2023Potentially unable to open forceps jaws when the endoscope s |
| FLEX. BIOPSY FORCEPS 5FR WL 550MM, Product Number 829.051Class IIMar 24, 2023Potentially unable to open forceps jaws when the endoscope s |
| FLEX. GRASP. FORCEPS 5FR WL 550MM, Product Number 828.051Class IIMar 24, 2023Potentially unable to open forceps jaws when the endoscope s |
| FLEX. GRASP. FORCEPS 6.6FR WL 550MM, Product Number 8736.685Class IIMar 24, 2023Potentially unable to open forceps jaws when the endoscope s |
| CUTTING ELECTRODE BIPO 24.5FR, REF 4653.1323Class IIJun 25, 2021Product labeled as Cutting Electrode may contain BIVAP elect |