20ml Transfix (2019-11-11)

TransFix Recall Summary TransFix 20ml vials have been recalled across Canada due to issues classified as a Class I medical device concern. The recall affects all TransFix 20ml products distributed in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2019-11-29
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/e7d75f72-ca3e-472e-96bb-46f8d4767791