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Healthmaxx Global Inc.
FDA recall F-1934-2013 · Class III · reported 2013-10-02 · Terminated
- Product
- MAX Brand Nitric Oxide Enhance, 90 Count Capsules Product labeling reads in part:"MAX Nitric Oxide Enhance***DIETARY SUPPLEMENT 90 Capsules***0 65176 55958 5***Manufactured in FDA Approved Facility for:HealthMax Products Co. Altadena, CA 91001***".
- Reason
- 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.
- Quantity
- 5,223 bottles
- Distribution
- CA, MD, and NY
- Firm location
- CA, United States
- Initiated
- Voluntary: Firm initiated
- First notice
- Letter
- Recall started
- 2013-06-10
- Terminated
- 2014-11-14
- Code info
- Lot # R1018 UPC 0 65176 55958 5
Source: U.S. Food and Drug Administration, openFDA Food Enforcement database (openFDA Food Enforcement, imported 2026-09). The FDA does not validate openFDA data for completeness or accuracy. This is a record of an enforcement action, not safety advice.