Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported January 16, 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&.
Possible inclusion of small metal fragments embedded within the tablets of Protandim Dietary Supplement.
Lifevantage Corp recalled Protandim is packaged in a 90cc cylindrical blue bottle with a silver cap and contains th… - a moderate-severity action.
Protandim is packaged in a 90cc cylindrical blue bottle with a silver cap and contains th… was recalled by Lifevantage Corp in January 16, 2013. Reason: Possible inclusion of small metal fragments embedded within the tablets of Protandim Dietary Supplement.. Check the official notice for the remedy. Verify recall #F-0876-2013 with the FDA Food before acting.
The recall
Lifevantage Corp issued this moderate-severity FDA Food recall-Possible inclusion of small metal fragments embedded within the tablets of Protandim Dietary Supplement..
- Moderate
- severity level
- Class II
- classification
- January 16, 2013
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-0876-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-0876-2013) was formally reported on January 16, 2013, with the manufacturer initiating the action on December 5, 2012. It is classified under Moderate severity (Class II), with a current status of Terminated. Lifevantage Corp is listed as the recalling firm, operating out of Sandy, UT. Federal records list the affected scope as 247,896 bottles.
The documented reason for this recall is: Possible inclusion of small metal fragments embedded within the tablets of Protandim Dietary Supplement. Distribution data in the federal record shows the product reached: 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 …. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Children & Baby Products recalls over time
Where this recall sits in its category - 3,731 children & baby products recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
247,896 bottles
Related Recalls
6
0 from same agency
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&.
Reason for recall
Possible inclusion of small metal fragments embedded within the tablets of Protandim Dietary Supplement.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-0876-2013 |
| Date reported | January 16, 2013 |
| Date initiated | December 5, 2012 |
| Recalling firm | Lifevantage Corp |
| Firm location | Sandy, UT |
| Affected scope | 247,896 bottles |
| Distribution | 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… |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-0876-2013) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
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&.. Recalled by Lifevantage Corp. Units affected: 247,896 bottles.
Why was this product recalled? ▼
Possible inclusion of small metal fragments embedded within the tablets of Protandim Dietary Supplement.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on January 16, 2013. Severity: Moderate. Recall number: F-0876-2013.
Where was the recalled product distributed? ▼
Distribution: 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..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-0876-2013) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
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Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported January 16, 2013. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.