Naconda Longer Leg Iliac Stent Graft Systems (2017-11-09)

Anaconda Longer Leg Iliac Stent Graft Systems Recall Medtronic is recalling Anaconda Longer Leg Iliac Stent Graft Systems used to treat abdominal aortic aneurysms because the device may not function as intended due to a manufacturing issue. The systems were distributed across Canada to hospitals and medical facilities. This is a Class I recall, which means there is a serious potential for adverse health consequences.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-11-24

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/42b4216c-600c-4fb3-ad47-1fc0a5edc7a7