Zenith Alpha Abdominal Endovascular Graft (2020-06-02)
Zenith Alpha Abdominal Endovascular Graft Recall The Zenith Alpha Abdominal Endovascular Graft, a medical device used to treat abdominal aortic aneurysms, has been recalled due to a defect that could affect how the device functions. The device was distributed across Canada. This recall affects patients who have received or may receive this specific graft as a treatment option.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2020-06-19
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/091c9532-eb47-43cd-ba6f-13199b38d73a