Optisite And Fem-flex II Arterial Perfusion Cannulas
OptiSite and Fem-Flex II Arterial Perfusion Cannulas are being recalled across Canada due to a performance issue. These medical devices are used for arterial perfusion during certain medical procedures. The recall affects all units distributed in Canada.
- Product
- OptiSite and Fem-Flex II Arterial Perfusion Cannulas
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2025-06-18
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/4dee41d6-6309-4804-ab66-34c804770931