Dxh 500 (2016-07-19)

DXH 500 Recall Summary The DXH 500 medical device has been recalled across Canada due to a Class I safety issue. This is the most serious type of recall, indicating the device could cause serious injury or death. The recall affects all units distributed in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2016-07-29
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/2b5a1ffa-91b0-49d8-a65f-eb15b47b37c5