Rapidflap System, 12mm - 20mm Rapidflap Spindown Clamp (2018-10-11)

RapidFlap System Recall The RapidFlap System SpinDown Clamp (12MM - 20MM models) is being recalled across Canada. The recall was initiated due to issues identified with this medical device. This recall affects all units of this product that were distributed in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2018-11-30
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/84de2e33-8f05-4161-ad44-39b7e77de02a