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Class II: temporary or reversible health riskTerminated

Lifevantage Protandim is packaged in a 90cc cylindrical Recall

Protandim is packaged in a 90cc cylindrical blue bottle with a silver cap and contains…

Lifevantage Corp · Sandy, UT

Risk level
Class II
Reported by FDA
Jan 16, 2013
Recall ID
F-0876-2013
Check your lot numberHow we source this data

Summary

Lifevantage recalled Protandim is packaged in a 90cc cylindrical starting Dec 5, 2012. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-0876-2013 on Jan 16, 2013. Reason: Possible inclusion of small metal fragments embedded within the tablets of Protandim Dietary Supplement. Status: Terminated.

Why it was recalled

Possible inclusion of small metal fragments embedded within the tablets of Protandim Dietary Supplement.

Product description

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&.

Lot numbers, UPCs & expiration codes

Lot # / Expiration Date: 12-0258 / 7/2/2015;12-0259 / 7/3/2015; 12-0292 / 7/9/2015; 12-0294 / 7/11/2015; 12-0295 / 7/12/2015; 12-0304 / 7/18/2015; 12-0306 / 8/16/2015; 12-0307 / 8/17/2015; 12-0373 / 8/21/2015; 12-0382 / 9/21/2015.

Where it was sold

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.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-0876-2013
Classification
Class II
Status
Terminated
Recall initiated
Dec 5, 2012
FDA report date
Jan 16, 2013
Quantity
247,896 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Lifevantage Corp

Original FDA data

Every field from FDA enforcement report F-0876-2013, exactly as published.

Show all FDA fields
City
Sandy
State
UT
Status
Terminated
Country
United States
Event ID
63826
Address
9815 Monroe St
Address (line 2)
STE 100
Code information
Lot # / Expiration Date: 12-0258 / 7/2/2015;12-0259 / 7/3/2015; 12-0292 / 7/9/2015; 12-0294 / 7/11/2015; 12-0295 / 7/12/2015; 12-0304 / 7/18/2015; 12-0306 / 8/16/2015; 12-0307 / 8/17/2015; 12-0373 / 8/21/2015; 12-0382 / 9/21/2015.
Postal code
84070-4296
Report date
Jan 16, 2013
Product type
Food
Recall number
F-0876-2013
Classification
Class II
Recalling firm
Lifevantage Corp
Product quantity
247,896 bottles
Termination date
May 23, 2014
Reason for recall
Possible inclusion of small metal fragments embedded within the tablets of Protandim Dietary Supplement.
Voluntary / mandated
Voluntary: Firm initiated
Product description
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&.
Distribution pattern
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.
Recall initiation date
Dec 5, 2012
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Jan 9, 2013

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0876-2013, published Jan 16, 2013. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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