K 200 Ultra S (2016-04-19)

Recall Summary The AK 200 ULTRA S medical device is being recalled across Canada due to a safety issue. This recall affects all units of this device distributed in Canada. The device has been classified as a Class I recall, which is the most serious category.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-05-09

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/f7ded792-1186-4bc1-80dc-bcae30ac08b5