Class IIITerminated in FDA datasetJun 10, 2013

Dietary Supplement labeled and packaged under the following: LIVERAID

Recalling firm: Healthmaxx Global Inc.

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.

Check the codes ↓

The exact 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***".

Check the codes

Compare these FDA-provided codes, lot numbers or dates with the product you have.

Match the product, size and code together. A similar name alone does not identify your batch.

Original FDA code information

Lot # LS122 UPC: 6 65176 82031 1, 6 65176 02434 4, and 0 65176 06068

TypeCode / valueContext
UPC665176820311Lot # LS122 UPC: 6 65176 82031 1, 6 65176 02434 4, and 0 65176 06068
lotLS122Lot # LS122 UPC: 6 65176 82031 1, 6 65176 02434 4, and 0 65176 06068

Recall details

Recall number
F-1921-2013
Event ID
65733
FDA status
Terminated
Initiated
Jun 10, 2013
Reported
Oct 2, 2013
Classified
Sep 24, 2013
Terminated
Nov 14, 2014
Quantity
5775 bottles
Location
Hacienda Heights, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

CA, MD, and NY

FDA source record · F-1921-2013

Data updated September 16, 2026. View official FDA data ↗

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.