Visudep-f Frozen Factors Deficient Plasma (2017-08-29)

Visudep-F Frozen Factors Deficient Plasma Recall Visudep-F Frozen Factors Deficient Plasma has been recalled across Canada due to a medical device issue. This product is used to treat bleeding disorders by replacing missing blood clotting factors. The recall affects all patients who may have received or could receive this product.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2017-09-26
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/33a5d5ba-908f-4e3e-8e0a-31289af257d0