Ferinject: labelled with the incorrect vial size on the outer carton.
Brand(s)
Last updated
Summary
Product
Ferinject
Issue
Health products - Labelling
What to do
Consult your healthcare provider prior to discontinuing use of the affected product(s), or for any health concerns.
Affected products
Brand |
Product Name |
Market Authorization |
Dosage Form |
Strength |
Lot |
|---|---|---|---|---|---|
Ferinject |
Ferinject |
DIN 02546078 |
Dispersion |
IRON (FERRIC CARBOXYMALTOSE) 50 mg/ml |
4621022EB, 4572022EA |
Issue
Affected lot(s) are labelled with the incorrect vial size on the outer carton.
What you should do
- Verify if your product is affected.
- Consult your healthcare provider prior to discontinuing use of the affected product(s), or for any health concerns.
- Contact the recalling firm if you have any questions about the recall.
- Report any health product related side effects to Health Canada.
- Report any other health product safety complaints to Health Canada.
Additional information
Background
Depth of recall: wholesalers
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Drugs
Companies
CSL Behring
350-55 Metcalfe Street,
Ottawa, ON, Canada
K1P 6L5
Published by
Health Canada
Audience
General public
Healthcare
Industry
Recall class
Type III
Identification number
RA-76898
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