Ferinject: Labelled With The Incorrect Vial Size On The Outer Carton.

Ferinject vials are being recalled across Canada because the outer carton label shows the wrong vial size. This is a Class I recall, which is the most serious classification. The affected product was distributed nationwide in Canada.

Product
Ferinject
Reason
Labelling
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DRUGS
Recall date
2025-02-04
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DRUGS

Recall details on Nibble Recalls: https://trynibble.app/recalls/3935cdf3-4bb0-4fa5-918d-65d3d05fecc2