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Amlodipine - 5 mg
- Starting date:
- May 24, 2013
- Posting date:
- June 6, 2013
- Type of communication:
- Drug Recall
- Subcategory:
- Drugs
- Hazard classification:
- Type II
- Source of recall:
- Health Canada
- Issue:
- Product Safety, Quality
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-33947
Recalled products
- Amlodipine - 5 mg
Reason
Quality concerns at the manufacturing facility of the active ingredients used in the products.
Depth of distribution
Distributed to wholesalers / pharmacies across Canada
Affected products
A. Amlodipine - 5 mg
DIN, NPN, DIN-HIM
DIN 02331284Dosage form
- Tablets
Strength
- 5 mg
Lot or serial number
- More than 10 numbers, contact manufacturer
Companies
- Recalling Firm
-
Sanis Health Inc.
333 Champlain Street, Suite 102
Dieppe
E1A 1P2
New Brunswick
CANADA
- Marketing Authorization Holder
-
Sanis Health Inc.
333 Champlain Street, Suite 102
Dieppe
E1A 1P2
New Brunswick
CANADA