Myndmove Functional Electrical Stimulater

Myndmove Functional Electrical Stimulator Recall Myndmove Functional Electrical Stimulators are being recalled across Canada because they don't meet safety and effectiveness requirements for medical devices. The devices were distributed in Canada without proper regulatory approval. This recall affects all users of the Myndmove Functional Electrical Stimulator.

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-03-10

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/60d37bf3-bdbe-4920-9c75-f98066bdf21c