Health product recall

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