Utocheck 5+ (2017-07-08)
Recall Summary AutoCheck 5+ blood glucose monitoring systems are being recalled in Canada due to a medical device issue. The recall affects all AutoCheck 5+ systems distributed across Canada. This is classified as a Class I recall, the most serious category.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2017-10-05
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/d1486adf-69a5-4509-a547-9a9c26896e7d