Femoral Arterial Cannula - Fem-flex II And Duraflo II Fem-flex II (2014-04-09)

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2014-05-05
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/c693c4ae-c858-42c9-97ba-d36d33a79b9f