Revolve System (2017-09-07)

Revolve System Recall Summary The Revolve System, a medical device distributed across Canada, has been recalled due to safety concerns. The recall is classified as Class I, indicating a serious potential health risk. The device was distributed nationwide in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-09-26

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/99d2c0e9-572c-4b1e-b9c7-71879d946811