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Healthmaxx Global Inc.
FDA recall F-1921-2013 · Class III · reported 2013-10-02 · Terminated
- Product
- Dietary Supplement labeled and packaged under the following: LIVERAID, 200 Count Softgels; LIVER AID, 200 Count Softgels; MAX Brand LIVER STRONG 200 Count Softgels. Product labeling reads in part:"LIVERAID***Dietary Supplement 200 Softgels***6 65176 82031 1***Manufactured in FDA Approved Facility For:HealthMax Products Co. Altadena, CA 91001***". Product labeling reads in part:"LIVER AID***DIETARY SUPPLEMENT 200 Softgels***6 65176 02434 4***Manufactured in FDA Approved Facility For:HealthMax Products Co. Altadena, CA 91001***". Product labeling reads in part:"MAX LIVER STRONG Dietary Supplement 200 Softgels***0 65176 06068***Manufactured in FDA Approved Facility For:HealthMax Products Co. Altadena, CA 91001***".
- Reason
- In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
- Quantity
- 5775 bottles
- Distribution
- CA, MD, and NY
- Firm location
- CA, United States
- Initiated
- Voluntary: Firm initiated
- First notice
- Letter
- Recall started
- 2013-06-10
- Terminated
- 2014-11-14
- Code info
- Lot # LS122 UPC: 6 65176 82031 1, 6 65176 02434 4, and 0 65176 06068
Source: U.S. Food and Drug Administration, openFDA Food Enforcement database (openFDA Food Enforcement, imported 2026-09). The FDA does not validate openFDA data for completeness or accuracy. This is a record of an enforcement action, not safety advice.