HF Resection Electrodes, Model Numbers WA22602S, WA22603S, WA22621S and WA22657S
FDA device recall Z-0424-2023 · posted 2022-12-07 · Open, Classified
Recall details
- Recalling firm
- Olympus Corporation of the Americas
- 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 procedure.
- Action taken
- On November 4, 2022, the firm notified affected customers. Customers were instructed to identify any affected product in their inventory. Affected product should be returned to Olympus, who will issue a credit to the customer upon return of affected product. Those who have distributed the devices outside their facility should notify their customers of this removal action immediately. To return product, contact your Olympus customer service representative at 1-800-848-9024.
- Root cause
- Packaging process control
- Status
- Open, Classified
- Product code
- FJL
- Quantity affected
- 186 boxes (930 pieces)
- Distribution
- US Nationwide domestic distribution.
- Date initiated
- 2022-11-04
- Date posted
- 2022-12-07
- Location
- Center Valley, PA
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| Resection Electrodes with HF cable (K171965) | Olympus Winter & Ibe GmbH | 2017-09-28 |