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Durazest (2016-02-05)
- Starting date:
- February 5, 2016
- Posting date:
- February 16, 2016
- Type of communication:
- Drug Recall
- Subcategory:
- Natural health products
- Hazard classification:
- Type I
- Source of recall:
- Health Canada
- Issue:
- Product Safety
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-57076
Affected products
Durazest
Reason
Durazest capsule lots recalled as a precautionary measure. Product used the same capsule shells found to be adulterated with Tadalafil in Forta for Men.
Depth of distribution
Retailers across Canada
Affected products
Durazest
DIN, NPN, DIN-HIM
NPN 80033381
Dosage form
Capsule
Strength
- Ginkgo biloba 50.0 mg
- Epimedium brevicornu 150.0 mg
- Lycium barbarum 80.0 mg
- Ophiocordyceps sinensis 120.0 mg
- Panax ginseng 100.0 mg
Lot or serial number
- Lot 230
- Lot 231
- Lot 232
- Lot 233
Companies
- Recalling Firm
-
Vivo Brand Management
3318 Second Street East
Cornwall
K6H 6J8
CANADA
- Marketing Authorization Holder
-
Vivo Brand Management
3318 Second Street East
Cornwall
K6H 6J8
CANADA