Carescape Respiratory Modules (2019-09-30)

GE CARESCAPE Respiratory Modules Recall GE's CARESCAPE Respiratory Modules are being recalled across Canada due to a defect in the medical device. This is a Class I recall, which indicates a serious issue. The recall affects respiratory monitoring equipment distributed throughout Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2019-11-01
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/c6cf3f2b-467b-434d-b21e-646731dbdf30