Dietary Supplements under the same formulation, Labeled and Packaged in the Following: MAX Brand Proste-Support, 150 Count Tablets. Product labeling reads in part:"Manufactured for: HealthMax Products Inc. Altadena, CA 91001***".

Recall Insight

This FDA Food action (record #F-1916-2013) was formally reported on October 2, 2013, with the manufacturer initiating the action on June 10, 2013. It is classified under Low severity (Class III), with a current status of Terminated. Healthmaxx Global Inc. is listed as the recalling firm, operating out of Hacienda Heights, CA. Federal records indicate 7,074 bottles units are affected.

The documented reason for this recall is: 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)ing… Distribution data in the federal record shows the product reached: CA, MD, and NY. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 13 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.