Life Rising — FDA Recall History & Enforcement Records
Data Notice: Recall frequency varies by category and firm size; data is comparative and may not indicate actual brand safety or quality. See Methodology.
As of July 22, 2026, Life Rising has 3 recorded FDA food enforcement actions in the openFDA database. Their most recent recall was on 28 Oct 2016. Life Rising is categorized under Supplements & Specialty based on their predominant recall history.
Recall activity over time for Life Rising
How serious are Life Rising recalls?
FDA recall classifications by severity
Full FDA recall history for Life Rising
All 3 FDA enforcement actions sourced from openFDA · Sorted by date, most recent first
| Date | Product | Reason | Class & Status |
|---|---|---|---|
| 28 Oct 2016Official FDA Notice | Life Rising TT Side Head Regulator, Chinese Herbal Supplement, 60 Tablets; Manufactured for: Ton Shen Health (USA), Chic | High levels of lead discovered in product. | Class ITerminated |
| 14 Sep 2016Official FDA Notice | Product is packaged in a white plastic bottle with green lettering. The label reads in part LIFE RISING, Chinese Herbal | The dietary supplement Brain ECM contains lead. | Class ITerminated |
| 1 Aug 2016Official FDA Notice | The product is packaged in a white plastic bottle with green lettering. The label reads in part “LIFE RISING DHZC-2, blo | The dietary supplement contains lead. | Class ITerminated |
Where have Life Rising recalls occurred?
States affected across all recorded FDA enforcement actions
Where does this recall data come from?
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Data sourced from the FDA Recall Enterprise System via openFDA API. This information is for educational purposes only and does not constitute health or legal advice. FoodRecallFinder.com is not affiliated with or endorsed by the U.S. Food and Drug Administration.
To determine if your specific product is affected, verify that the brand name, product description, lot number, UPC code, and date range all match the recall details exactly. When in doubt contact the recalling firm or visit FDA.gov.
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