Viibryd Starter Kit (10 & 20 mg)
- Starting date:
- May 7, 2018
- Type of communication:
- Drug Recall
- Subcategory:
- Drugs
- Hazard classification:
- Type II
- Source of recall:
- Health Canada
- Issue:
- Product Safety
- Audience:
- Healthcare Professionals
- Identification number:
- RA-66756
Recalled Products
Viibryd Starter Kit (10 & 20 mg)
Reason
Affected lots are labelled with the incorrect strengths on the blister card.
Depth of distribution
Distributed to doctors in BC, AB, SK, ON, QC, NB, NS
Affected products
Viibryd Starter Kit (10 & 20 mg)
DIN, NPN, DIN-HIM
DIN 02443759
Dosage form
Kit, Tablet
Strength
10 & 20 mg
Lot or serial number
- 10 mg: 1540126
- 20 mg: 1540126
Companies
- Recalling Firm
-
Allergan Inc.
85 Enterprise Blvd, Suite 500
Markham
L6G 0B5
Ontario
CANADA
- Marketing Authorization Holder
-
Forest Laboratories Canada Inc.
500-85 Enterprise Blvd
Markham
L6G 0B5
Ontario
CANADA