Liko M220 / M230 Mobile Lift

Liko M220 / M230 Mobile Lift Recall Liko M220 and M230 mobile lifts are being recalled across Canada due to an increased risk of adverse events. These devices are used to assist with patient handling and mobility. The recall affects all units distributed in Canada.

Product

Liko M220 / M230 Mobile Lift

Reason

Increased risk or new adverse events

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2022-01-24

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/3458aee2-d2ee-43f6-82d3-49c066c4d615