Ultrafilter U9000 (2018-02-27)

Ultrafilter U9000 Recall Summary The Ultrafilter U9000 medical device has been recalled across Canada due to a safety concern. This is a Class I recall, which indicates a serious issue. The device was distributed throughout Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-03-19

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/0532f46f-e2c4-4e45-afac-3107792921a8