Prestige Vh (2017-12-01)

Prestige VH Recall Summary Prestige VH medical devices are being 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 the device's medical function, though further details about the particular safety issue are not provided in this notice. This recall affects all Prestige VH devices distributed in Canada as of December 1, 2017.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-12-21

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/50ed1b2f-e3a9-4136-a305-598e1caf372b