Zenith Alpha Spiral-z Endovascular Leg (2020-01-14)
Zenith Alpha Spiral-Z Endovascular Leg Recall The Zenith Alpha Spiral-Z Endovascular Leg, a medical device used in vascular procedures, has been recalled in Canada. The device was classified as a Class I recall, meaning there is a serious potential for adverse health effects. The recall affects products distributed across Canada.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2020-01-31
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/d4e64376-88f7-43e1-8949-22d07ed759eb