Utaswako Dcp And Utaswako Afp-l3 (2018-07-27)

uTASWako DCP and uTASWako AFP-L3 Recall uTASWako DCP and uTASWako AFP-L3 medical devices are being recalled across Canada. These are Class I recalls, which means the devices could cause serious health problems or death. The recall affects medical devices distributed throughout Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2018-08-31
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/e84e1dd8-43ab-490f-9c71-a600980de5b7