Protandim is packaged in a 90cc cylindrical blue bottle with a silver cap and contains thirty caplets per bott

Recall map → All recalls → F-0876-2013

Protandim is packaged in a 90cc cylindrical blue bottle with a silver cap and contains thirty caplets per bottle. Label has a blue background with multi-colored print and pictorial stating in part: Lifevantage PROTANDIM *the Nrf2 Synergizer Dietary Supplement I 30 Caplets&amp;amp;amp;amp;amp;amp;amp;amp;. Lifevantage Corp · reported 2013-01-16

Terminated This recall has been closed out by the agency.

Reason for recall: Possible inclusion of small metal fragments embedded within the tablets of Protandim Dietary Supplement.
Classification: Class II
Recall initiated: 2012-12-05
Reported by the agency: 2013-01-16
Closed out (terminated): 2014-05-23
Recalling firm: Lifevantage Corp
Sandy, UT
United States
This is the firm that issued the recall — commonly a distributor or processor. It is not the origin of contamination.
Distribution (the agency's own words): Sale of products through a network of independent distributors, preferred customers and end consumers in the United States, Japan, Australia and Mexico. Sales also directly to end consumers for personal consumption in Canada. Independent distributors consume the product themselves and in some cases sell the product or provide the product gratis to those potentially interested in LifeVantage. Preferred customers purchase the products on a monthly, auto-ship basis directly from Life Vantage. Other end consumers purchase directly from LifeVantage via the website and are assigned to a distributor.
States we parsed from that text: could not be parsed
No state list could be read from the agency's text. Absence here is not evidence the product stayed put.
Food category: Dietary supplementsderived
Assigned by a reviewed keyword rulebook over the product description, not by the agency.
Recall type: Voluntary: Firm initiated
Recall number: F-0876-2013

This page reproduces a record published by the US Food and Drug Administration. It is not real-time: recalls typically appear in FDA's Enforcement Report weeks after they begin — a median of 40 days, see publication lag. For current food safety information consult FDA and USDA FSIS directly.