Dietary Supplement labeled and packaged under the following: LIVERAID, 200 Count Softgels; LIVER AID, 200 Cou

Recall map → All recalls → F-1921-2013

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:"LIVERAIDDietary Supplement 200 Softgels6 65176 82031 1Manufactured in FDA Approved Facility For:HealthMax Products Co. Altadena, CA 91001". Product labeling reads in part:"LIVER AIDDIETARY SUPPLEMENT 200 Softgels6 65176 02434 4Manufactured in FDA Approved Facility For:HealthMax Products Co. Altadena, CA 91001". Product labeling reads in part:"MAX LIVER STRONG Dietary Supplement 200 Softgels0 65176 06068Manufactured in FDA Approved Facility For:HealthMax Products Co. Altadena, CA 91001***". Healthmaxx Global Inc. · reported 2013-10-02

Terminated This recall has been closed out by the agency.

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.
Classification: Class III
Recall initiated: 2013-06-10
Reported by the agency: 2013-10-02
Closed out (terminated): 2014-11-14
Recalling firm: Healthmaxx Global Inc.
Hacienda Heights, CA
United States
This is the firm that issued the recall — commonly a distributor or processor. It is not the origin of contamination.
Distribution (the agency's own words): CA, MD, and NY
States we parsed from that text: CA MD NY
The agency named these states. Parse method explicit_state_list, confidence high.
Food category: Dietary supplementsderived
Assigned by a reviewed keyword rulebook over the product description, not by the agency.
Recall type: Voluntary: Firm initiated
Recall number: F-1921-2013

This page reproduces a record published by the US Food and Drug Administration. It is not real-time: recalls typically appear in FDA's Enforcement Report weeks after they begin — a median of 40 days, see publication lag. For current food safety information consult FDA and USDA FSIS directly.