Discovery Igs 730/740 System (2016-04-18)

Recall Summary The Discovery IGS 730/740 System has been recalled across Canada due to a medical device issue. This system is used in medical settings and has been classified as a Class I recall, indicating a serious safety concern. The recall affects all units distributed throughout Canada since the product's introduction.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2016-05-16
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/f8ad27aa-4c70-4162-aab9-05212d083b09