Ngiojet Ultra 5000a Console (2019-11-11)

Angiojet Ultra 5000a Console Recall The Angiojet Ultra 5000a Console, a medical device used in Canada, has been recalled due to a safety issue. This recall affects all units of this device distributed across Canada. The recall is classified as Class I, indicating a serious potential health risk.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-12-13

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/e336531f-3f20-4c8a-88a4-70fdde919dd1