Veriq And Veriq C System (2018-05-04)

VeriQ and VeriQ C System Recall Summary The VeriQ and VeriQ C System medical devices are being recalled across Canada. The recall is classified as Class I, indicating a serious issue with the devices. The specific reason for the recall relates to the device's medical function, though additional details about the particular safety concern are not provided in this notice.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-06-01

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/6a0afbc0-3e3d-41d8-bd41-ef103fc0ab83