Navitracker Kit A : Knee

Navitracker Kit A: Knee Recall Summary Navitracker Kit A for knee procedures is being recalled in Canada due to an increased risk of adverse events. The recall applies to all Navitracker Kit A: Knee products distributed across Canada. This is classified as a Class I recall, indicating a serious safety concern.

Product
Navitracker Kit A : Knee
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/dfc79677-b574-45ab-83ec-805bf68dc75c