Q-rad System (2019-03-30)

Q-Rad System Recall Summary The Q-Rad System medical device is being recalled across Canada due to a safety or effectiveness issue classified as Class I, meaning there is a reasonable probability that use of the device could cause serious adverse health consequences or death. This recall affects all Q-Rad System devices distributed in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-04-05

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/290a5771-b8f7-49b5-b182-bb4adcafe4de