Utocheck 5+ (2017-09-21)

AutoCheck 5+ Recall Summary AutoCheck 5+ medical devices distributed across Canada are being recalled due to a Class I issue. The specific reason for the recall relates to a defect or problem with the device itself, though the exact nature of the issue is not detailed in this notice. This recall affects all AutoCheck 5+ devices that were distributed in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2017-10-06
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/0629a641-26e9-4f3b-9163-f4f5727f6995