Quickdraw 22 & 25 Venous Cannula (2019-12-17)

QuickDraw 22 & 25 Venous Cannula Recall The QuickDraw 22 and 25 venous cannulas (medical devices used to access veins) have been recalled across Canada. The devices are classified as a Class I recall, indicating a serious health concern. This recall affects all Canadian users of these specific cannula models.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2020-01-10
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/f5bb0f8c-ccae-46c0-a9b1-e295626fa8d4