MAX Brand LIVERAID — Class III food recall F-1922-2013
Terminated recall by Healthmaxx Global Inc., reported 2013-10-02, distributed in CA, MD, NY. In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due t
| Recall number | F-1922-2013 |
|---|---|
| Product type | Food |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Healthmaxx Global Inc., Hacienda Heights, CA, United States |
| Recall initiated | 2013-06-10 |
| Classified | 2013-09-24 |
| Reported by FDA | 2013-10-02 |
| Terminated | 2014-11-14 |
| Distributed | CA, MD, NY |
| Quantity | 3,197 bottles |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00665176351686 |
| Lot numbers | L0126 |
Product
MAX Brand LIVERAID, 200 Count Bottle. Product labeling reads in part:"MAX LIVERAID Dietary Supplement 200 Counts***6 65176 35168 6***Manufactured in FDA Approved Facility For:HealthMax Products Co. Altadena, CA 91001***".
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-1922-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.