Foquest Capsule (2018-08-08)
- Starting date:
- August 8, 2018
- 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-67532
Recalled Products
Foquest Capsule
Reason
Affected lot had an out of specification result for potency during shelf life testing.
Depth of distribution
Wholesalers
Affected products
Foquest Capsule
DIN, NPN, DIN-HIM
DIN 02470322
Dosage form
Capsule (Controlled Release)
Strength
Methylphenidate Hydrochloride 55mg
Lot or serial number
135570
Companies
- Recalling Firm
-
Purdue Pharma
575 Granite Court
Pickering
L1W 3W8
Ontario
CANADA
- Marketing Authorization Holder
-
Purdue Pharma
575 Granite Court
Pickering
L1W 3W8
Ontario
CANADA