Ccumab Plus Bordetella Pertussis /parapertussis Dfa (2014-03-01)

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2015-05-21
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/2204fd71-1441-448f-b178-01b51bf2e248