Rjohuntleigh Sara 3000, Sara Plus, Tenor, Minstrel (2017-10-31)

Recall Summary ArjoHuntleigh is recalling Sara 3000, Sara Plus, Tenor, and Minstrel patient lift devices distributed across Canada due to a medical device issue. The recall is classified as Class I, indicating a serious safety concern. This recall affects all users of these lift device models in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-11-30

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/4b355239-203b-446e-a4c7-a2879e9ff120