MAX Brand GOUT AID, 130 Count Tablets Product labeling reads in part:"MAX GOUT AID***Dietary Supplement 130 Tablets***6 0 65176 26512 7***HealthMax Products Co. Altadena, CA 91001***".

Healthmaxx Global INC. recalled MAX Brand GOUT AID, 130 Count Tablets in a Class III action, the FDA tier used when a product is unlikely to cause adverse health effects, typically for labeling or minor regulatory issues on Jun 10, 2013.

The recall cites a labeling or packaging error: "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." Labeling defects matter most when the wrong label conceals an ingredient a consumer is trying to avoid.

The product reached multiple states, recorded by the FDA as "CA, MD, and NY." A multi-state footprint means the same lot can surface in households far from the producer. The recalling firm is based in Hacienda Heights, CA. The recall covers 2,245 bottles of product. The FDA has Terminated this recall (first reported Oct 2, 2013), its final lifecycle state, indicating the agency considers the corrective action resolved. The historical record remains useful for tracking a brand's recall pattern over time.