Interstim Percutaneous Extension
Interstim Percutaneous Extension Recall The Interstim Percutaneous Extension is being recalled across Canada due to an increased risk of adverse events. This product is used as part of a nerve stimulation system. The recall affects all Interstim Percutaneous Extension units distributed in Canada.
- Product
- Interstim Percutaneous Extension
- Reason
- Increased risk or new adverse events
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2022-01-24
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/532d39c3-f214-4755-b6d7-8426a0c484cc