Footswitch (accessory To Cusa Clarity System) (2017-09-26)

Recall Summary A footswitch accessory used with the CUSA Clarity surgical system has been recalled across Canada. The footswitch can fail to respond to foot commands during surgery, potentially leaving the device running unintentionally. This recall affects medical facilities and hospitals in Canada that use this surgical equipment.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-10-13

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/fdb46d47-eeea-44c3-b73c-1b1617ae7aa1