Scorpio Patella Assembly Instrument (2016-08-02)

Recall Summary The Scorpio Patella Assembly Instrument has been recalled across Canada due to issues with the medical device itself. This instrument is used in orthopedic surgical procedures and the recall affects all units that were distributed in Canada. The device has been classified as a Class I recall, which is the most serious type.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-08-19

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/12f322ae-0bbd-47b8-afdc-89949941382c