This page has been archived on the Web
Information identified as archived is provided for reference, research or recordkeeping purposes. It is not subject to the Government of Canada Web Standards and has not been altered or updated since it was archived. Please contact us to request a format other than those available.
Aerius Dual Action 12 Hour (2017-07-17)
- Starting date:
- July 17, 2017
- Posting date:
- October 4, 2017
- Type of communication:
- Drug Recall
- Subcategory:
- Drugs
- Hazard classification:
- Type III
- Source of recall:
- Health Canada
- Issue:
- Product Safety
- Audience:
- General Public, Hospitals, Healthcare Professionals
- Identification number:
- RA-64702
Affected products
Aerius Dual Action 12 Hour
Reason
Affected product was stored outside of the recommended storage conditions.
Depth of distribution
Retail stores/pharmacies in Manitoba, Saskatchewan, Alberta and Ontario
Affected products
Aerius Dual Action 12 Hour
DIN, NPN, DIN-HIM
DIN 02309300
Dosage form
Tablet (Extended-Release)
Strength
- Desloratadine 2.5mg
- Pseudoephedrine Sulfate 120mg
Lot or serial number
EXP 01/2018
Product UPC
UPC 056219332302
Companies
- Recalling Firm
-
Kohl & Frisch Limited (Distributor)
1750 Inkster Boulevard
Winnipeg
R2X IR4
Manitoba
CANADA
- Marketing Authorization Holder
-
Sandoz Canada Inc.
145 Jules-Léger
Boucherville
J4B 7K8
Quebec
CANADA