CUTTING ELECTRODE BIPO 24 — Class II medical device recall Z-2246-2021
Terminated recall by Richard Wolf GmbH, reported 2021-08-18, distributed nationwide. Product labeled as Cutting Electrode may contain BIVAP electrode.
| Recall number | Z-2246-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Richard Wolf GmbH, Knittlingen, N/A, Germany |
| Recall initiated | 2021-06-25 |
| Classified | 2021-08-11 |
| Reported by FDA | 2021-08-18 |
| Terminated | 2024-01-05 |
| Distributed | Nationwide (US) |
| Quantity | 20 boxes |
| Reason classes | labeling |
| Lot numbers | 21002858 |
| Model numbers | 4653.1323 |
Product
CUTTING ELECTRODE BIPO 24.5FR, REF 4653.1323
Reason for recall
Product labeled as Cutting Electrode may contain BIVAP electrode.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2246-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.