Wet-field Coagulator (2018-02-09)

Wet-Field Coagulator Recall Summary A medical device called a Wet-Field Coagulator has been recalled across Canada due to a safety concern. This device is used during surgical procedures to control bleeding. The recall is classified as Class I, which means there is a potential for serious injury or death.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2018-02-22
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/8304d0ec-bae4-4441-ab8f-e08b13a5f896