Recalls / Class III
Class IIIF-1928-2013
Product
Dietary Supplements Under the Same Formulation, Labeled and Packaged as 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***Manufactured in FDA Approved Facility for:HealthMax Products Co. Altadena, CA 91001***". Product labeling reads in part:"MAX LIVER STRONG***Dietary Supplment 200 Softgels***0 65176 06068 5***Manufactured in FDA Approved GMP Facility for:HealthMax Products Co. Altadena, CA 91001***".
- Type
- Food
- Affected lot / code info
- Lot # LS1227 UPCs: 6 65176 82031 1, 6 65176 02434 4, and 0 65176 06068 5
- Quantity
- 5775 bottles
Why it was recalled
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.
Recalling firm
- Firm
- Healthmaxx Global Inc.
- Notification channel
- Letter
- Type
- Voluntary: Firm initiated
- Address
- 16231 Elza Dr., N/A, Hacienda Heights, California 91745
Distribution
- Distribution pattern
- CA, MD, and NY
Timeline
- Recall initiated
- 2013-06-10
- FDA classified
- 2013-09-24
- Posted by FDA
- 2013-10-02
- Terminated
- 2014-11-14
- Status
- Terminated
Source: openFDA Food Enforcement endpoint. Recall record F-1928-2013. The FDA issues recall classifications as health-hazard assessments, not legal findings.