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Apo-K
- Starting date:
- May 31, 2013
- Posting date:
- June 20, 2013
- Type of communication:
- Drug Recall
- Subcategory:
- Drugs
- Hazard classification:
- Type II
- Source of recall:
- Health Canada
- Issue:
- Product Safety
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-34265
Recalled products
- Apo-K
Reason
Tablets may contain metal particles in the tablet coating.
Depth of distribution
Wholesalers, Pharmacies, Hospitals and one government consignee. All provinces.
Affected products
A. Apo-K
DIN, NPN, DIN-HIM
NPN 00602884Dosage form
- Slow Release Tablet
Strength
- 600 mg
Lot or serial number
100 Tablet Bottle:
- JP0376
1000 Tablet Bottle:
- JP0379
- JP0380
- JP0385
Companies
- Recalling Firm
-
Apotex Inc.
150 Signet Drive
Toronto
M9L 1T9
Ontario
CANADA
- Marketing Authorization Holder
-
Apotex Inc.
150 Signet Drive
Toronto
M9L 1T9
Ontario
CANADA