Healthmaxx Global Inc.: Food Recall in 2013 - (Recall #: F-1921-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

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***".

Product Classification:

Class III

Date Initiated: June 10, 2013

Date Posted: October 2, 2013

Recall Number: F-1921-2013

Event ID: 65733

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.

Status: Terminated

Product Quantity: 5775 bottles

Code Information:

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

Distribution Pattern:

CA, MD, and NY

Voluntary or Mandated:

Voluntary: Firm initiated