Sequestra 1000 System (2018-11-26)

Sequestra 1000 System Recall Summary The Sequestra 1000 System has been recalled across Canada due to concerns with the medical device. This is classified as a Class I recall, which indicates a serious issue. The recall affects all units of this device distributed throughout Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-01-08

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/51baa1c2-7050-4ace-a4e0-153d6376c0c1