Micafungin Sodium for Injection 50 mg/vial and 100 mg/vial: Linear barcode printed on the vial label is non-functioning
Last updated
Summary
Product
Micafungin Sodium for Injection 50 mg/vial and 100 mg/vial
Issue
Health products - Labelling
What to do
Consult your health care professional if you have any health concerns.
Distribution
Alberta
British Columbia
Ontario
Affected products
Brand |
Product Name |
Market Authorization |
Dosage Form |
Strength |
Lot |
|---|---|---|---|---|---|
Micafungin Sodium for Injection 50 mg/vial |
Micafungin Sodium for Injection 50 mg/vial |
DIN 02524953 |
Powder for Solution |
Micafungin Sodium 50 MG |
P03532F |
Micafungin Sodium for Injection 100 mg/vial |
Micafungin Sodium for Injection 100 mg/vial |
DIN 02524961 |
Powder for Solution |
Micafungin Sodium 100 MG |
P03544A |
Issue
Linear barcode printed on the vial label is non-functioning.
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
Juno Pharmaceuticals
Corp. 402 - 2233 Argentia Road, Mississauga
ON, L5N 2X7
Published by
Health Canada
Audience
General public
Healthcare
Industry
Distribution
Alberta
British Columbia
Ontario
Recall class
Type III
Identification number
RA-74163
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