FDA Device recall Z-0424-2023
HF Resection Electrodes, Model Numbers WA22602S, WA22603S, WA22621S and WA22657S
- FDA Device
- Class II
- ongoing
- Published 2022-12-14
On 2022-12-14 the FDA classified a Class II recall of HF Resection Electrodes, Model Numbers WA22602S, WA22603S, WA22621S and WA22657S by Olympus, citing an incompatible HF cable may be packaged with the HF Resection Electrodes. This cable cannot be connected to the electrosurgical generator and may lead to delay or cancellation of….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0424-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-11-04 |
| Published | 2022-12-14 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Olympus |
| Distribution | US |
Product
HF Resection Electrodes, Model Numbers WA22602S, WA22603S, WA22621S and WA22657S
Reason
An incompatible HF cable may be packaged with the HF Resection Electrodes. This cable cannot be connected to the electrosurgical generator and may lead to delay or cancellation of the surgical procedure.
Identifiers
| code_info | Model Number/ UDI-DI/ Lot Number WA22602S 14042761085127 1000090824 WA22603S 14042761085134 1000092201 WA22621S 1404276…Model Number/ UDI-DI/ Lot Number WA22602S 14042761085127 1000090824 WA22603S 14042761085134 1000092201 WA22621S 14042761085172 1000080316 WA22657S 14042761085301 1000092202 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0424-2023%22
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