M-Pregabalin 25mg Capsules (2019-08-21)
- Starting date:
- August 21, 2019
- Type of communication:
- Drug Recall
- Subcategory:
- Drugs
- Hazard classification:
- Type III
- Source of recall:
- Health Canada
- Issue:
- Product Safety
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-70931
Last updated: 2019-09-06
Summary
-
Product:
M-Pregabalin
Reason
The assay is out of specification in the affected lot.
Depth of distribution
Wholesalers
Affected products
M-Pregabalin
DIN, NPN, DIN-HIM
DIN 02467291
Dosage form
Capsule
Strength
Pregabalin 25mg
Lot or serial number
1805001965
Companies
- Recalling Firm
-
Marcan Pharmaceuticals Inc.
2 Gurdwara Rd.- Suite #112
Ottawa
K2E 1A2
Ontario
CANADA
- Marketing Authorization Holder
-
Mantra Pharma Inc.
9150 Leduc Boulevard, Suite 201
Brossard
J4Y OE3
Quebec
CANADA