Class II — Richard Wolf GmbH
| Recalling firm | RICHARD WOLF GMBH |
|---|---|
| Registered facility | View this company's 2 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Product labeled as Cutting Electrode may contain BIVAP electrode. |
| Product | CUTTING ELECTRODE BIPO 24.5FR, REF 4653.1323 |
| Quantity | 20 boxes |
| Distribution | US Nationwide Distribution in the states of CA, CO, IN, MA, NH |
| Initiated | 2021-06-25 |
| Classified | 2021-08-11 |
| Terminated | 2024-01-05 |
| Recall number | Z-2246-2021 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Richard Wolf GmbH (Z-2246-2021).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/88249/
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