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Citalopram-10, Methylphenidate recall (2014-07-08)
- Starting date:
- July 8, 2014
- Posting date:
- July 17, 2014
- Type of communication:
- Drug Recall
- Subcategory:
- Drugs
- Hazard classification:
- Type I
- Source of recall:
- Health Canada
- Issue:
- Product Safety
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-40677
Recalled Products
- Citalopram-10
- Methylphenidate
Reason
The recall of lot #481820 was initiated following the discovery of two bottles of the product Methylphenidate (5 mg) labelled as Citalopram-10. It was confirmed that the two bottles contained Methylphenidate (5 mg).
Depth of distribution
Wholesalers and pharmacies in Quebec
Affected products
A. Citalopram-10
DIN, NPN, DIN-HIM
DIN 02325047
Dosage form
- Tablet
Strength
- 10 mg
Lot or serial number
- Lot # 481820
Companies
- Recalling Firm
-
Pro Doc Ltd.
2925 Industrial Blvd.
Laval
H7L 3W9
CANADA
- Marketing Authorization Holder
-
Pro Doc Ltd.
2925 Industrial Blvd.
Laval
H7L 3W9
CANADA
B. Methylphenidate
DIN, NPN, DIN-HIM
DIN 02326221
Dosage form
- Tablet
Strength
- 5 mg
Lot or serial number
- Lot # 481820
Companies
- Recalling Firm
-
Pro Doc Ltd.
2925 Industrial Blvd.
Laval
H7L 3W9
CANADA
- Marketing Authorization Holder
-
Pro Doc Ltd.
2925 Industrial Blvd.
Laval
H7L 3W9
CANADA