Rkon Anesthesia System

Arkon Anesthesia System Recall Summary Arkon Anesthesia Systems are being recalled across Canada due to a defect that could affect the delivery of anesthesia during medical procedures. The systems may not function as intended, potentially putting patients at risk during surgery or other procedures requiring anesthesia. This recall affects all Arkon Anesthesia Systems distributed in Canada.

Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2017-03-16
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/4044354f-3401-45dc-b0ae-a5ada2e8abff