Protandim Supplement (Lifevantage) – Metal Fragment Risk (2012)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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&.
Brand
Lifevantage Corp
Lot Codes / Batch Numbers
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.
Products Sold
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.
Lifevantage Corp is recalling Protandim is packaged in a 90cc cylindrical blue bottle with a silver cap and contains thirty caplet due to Possible inclusion of small metal fragments embedded within the tablets of Protandim Dietary Supplement.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Possible inclusion of small metal fragments embedded within the tablets of Protandim Dietary Supplement.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 12, 2026