FDA Device recall Z-2246-2021
CUTTING ELECTRODE BIPO 24.5FR, REF 4653.1323
- FDA Device
- Class II
- terminated
- Published 2021-08-18
On 2021-08-18 the FDA classified a Class II recall of CUTTING ELECTRODE BIPO 24.5FR, REF 4653.1323 by Richard Wolf, citing product labeled as Cutting Electrode may contain BIVAP electrode.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2246-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-06-25 |
| Published | 2021-08-18 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Richard Wolf |
| Distribution | US |
Product
CUTTING ELECTRODE BIPO 24.5FR, REF 4653.1323
Reason
Product labeled as Cutting Electrode may contain BIVAP electrode.
Identifiers
| code_info | Lot Number 21002858 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2246-2021%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.