Hexapod Evo Module (2018-05-14)

HexaPOD evo Module Recall Summary The HexaPOD evo Module medical device has been recalled across Canada due to a safety concern classified as Class I, the most serious type of recall. The specific reason for the recall relates to a defect or malfunction in the device. This recall affects all HexaPOD evo Module devices distributed in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2018-05-25
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/bf26d89b-2966-40fe-b01e-9aad62edd203