Iguide Software 2.x Including Workstation (2019-07-16)

iGuide Software 2.x Recall Summary iGuide Software 2.x, including Workstation, is being recalled across Canada because it is classified as a medical device that does not meet regulatory requirements. This recall is classified as Class I, which is the most serious type. The recall affects all users of this software version in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-08-02

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/aa6d9e9a-53d5-4f4f-bfad-0b1e4e0af2a5