Id-diacell (2017-02-06)

ID-Diacell Recall Summary ID-Diacell medical devices are being recalled across Canada due to a quality or safety issue classified as Class I, the most serious type of recall. The specific reason for the recall relates to the medical device itself, though additional details are not provided in this notice. This recall affects consumers across Canada who may have this product.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2017-03-24
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/5c881db0-acd8-4558-94c1-5617900bf213