Carestation 620 And 650 (2017-05-02)

Carestation 620 and 650 Recall Summary Carestation 620 and 650 anesthesia delivery machines have been recalled across Canada due to a medical device issue. This recall affects healthcare facilities that use these machines. The FDA classified this as a Class I recall, indicating a serious problem with the device.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2017-06-12
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/3d788ef0-6393-493e-be7a-bc9eb1692769