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 certain abdominal aortic conditions, has been recalled across Canada. The recall is classified as Class I due to concerns with the device itself. This affects patients who received or may receive this graft.

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/ecaf848d-911b-4cca-b24d-7e41efa769c4