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Health product recall

Durazest

Starting date:
January 1, 2011
Posting date:
December 20, 2010
Type of communication:
Drug Recall
Subcategory:
Drugs
Hazard classification:
Type I
Source of recall:
Health Canada
Issue:
Undeclared Substance
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-2010A275

Recalled products

  1. Durazest

Reason

Product contains undeclared schedule F analogue.

Depth of distribution

Distributors and retailers across Canada. Distributors in US.

Affected products

Durazest

DIN, NPN, DIN-HIM
No Market Authorization
Dosage form
  • Capsules
Strength
  • 500 mg capsules
Lot or serial number
  • 717
  • 201
  • 205
  • 211
  • 212
  • 216
Companies
Recalling Firm
Natural Performance Products Ltd. 3680 Lamond Ave., Richmond, British Columbia V7E 1C6
Marketing Authorization Holder
N/A
Recalling Firm
Natural Performance Products Ltd.
3680 Lamond Ave.,
Richmond
V7E 1C6
Alberta
CANADA
Marketing Authorization Holder
Natural Performance Products Ltd.
3680 Lamond Ave.,
Richmond
V7E 1C6
Alberta
CANADA

Date modified: