Radrex-i (2018-09-12)

RADREX-i Recall Summary RADREX-i, a medical device distributed across Canada, has been recalled due to a Class I safety issue. The recall affects all Canadian consumers who may have this device. [Note: The specific reason for the Class I classification is not detailed in the information provided, so I cannot state the particular safety concern.]

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2018-09-28
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/3fffe237-ee37-4443-ac02-eb61155ed8ac