Healthmaxx Global Dietary Supplement labeled and packaged 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.

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***".

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

CA, MD, and NY

• Compare the brand, size, and lot/UPC codes on your package with the codes above.
• If it matches, don't eat it. Return it to the store for a refund or throw it away.
• Wash surfaces and containers that touched the product.
• If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall number

F-1921-2013

Classification

Class III

Status

Terminated

Recall initiated

Jun 10, 2013

FDA report date

Oct 2, 2013

Quantity

5775 bottles

Recall type

Voluntary: Firm initiated

Recalling firm

Healthmaxx Global Inc.