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