Da Vinci Si 5 X 300 Mm Curved Canula - Arm 1 And Arm 2 (2014-02-28)

Recall Summary Da Vinci SI 5 x 300 mm curved canulas (Arm 1 and Arm 2) are being recalled across Canada due to a medical device issue. This recall applies to all units distributed in Canada. The recall is classified as Class I, which is the most serious level of recall classification.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2014-04-30
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/ac903f69-f646-4df2-a51c-dec7e1529b09