Hemosil Factor XII Deficient Plasma (2017-07-17)

Recall Summary HemosIL Factor XII Deficient Plasma has been recalled across Canada due to a medical device issue. This product is used in laboratory testing to measure blood clotting. The recall affects all patients and healthcare facilities that have received this product in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-03-13

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/7e76e52e-9ad6-44e0-bde6-69278940d76e