F-1928-2013 Class III Terminated
Recall Details
- Product Type
- Food
- Report Date
- October 2, 2013
- Initiation Date
- June 10, 2013
- Termination Date
- November 14, 2014
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 5775 bottles
Product Description
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***".
Reason for Recall
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.
Distribution Pattern
CA, MD, and NY
Code Information
Lot # LS1227 UPCs: 6 65176 82031 1, 6 65176 02434 4, and 0 65176 06068 5