Hospira Mednet(2017-10-19)

Hospira MedNet Recall Summary Hospira MedNet medical devices were recalled across Canada due to a safety issue with the device itself. This is a Class I recall, which is the most serious type. The recall affects Hospira MedNet devices that were distributed throughout Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2017-11-10
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/9b612ad0-cd44-4131-8a28-19ed8e2acabf