Drug recall
HF Resection Electrodes, Model Numbers WA22602S, WA22603S, WA22621S and WA22657S
FDA recall event 91100 · Class II · Olympus Corporation of the Americas
Key facts
| Event ID | 91100 |
|---|---|
| Recall numbers | Z-0424-2023 |
| Recalling firm | Olympus Corporation of the Americas |
| Product type | Devices |
| Products | HF Resection Electrodes, Model Numbers WA22602S, WA22603S, WA22621S and WA22657S |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | 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… |
| Initiation date | Nov 4, 2022 |
| Report date | Dec 14, 2022 |
| City | Center Valley |
| State | PA |
| Country | United States |
| FEI number | 2429304 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: