Healthmaxx Global Recalls MAX Nitric Oxide Enhance Due to Mislabeling
Healthmaxx Global Inc. is voluntarily recalling MAX Brand Nitric Oxide Enhance dietary supplements because the label does not match the actual product or ingredients.
The agency’s classification
FDA (Food): Class III
Class III is a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 1/5 (Low).
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: The FDA classified this as a Class III recall, which by definition is unlikely to cause adverse health consequences, fitting the 'Low' severity criteria for documentation or labeling issues.
Plain-English summary
Healthmaxx Global Inc. is voluntarily recalling 5,223 bottles of MAX Brand Nitric Oxide Enhance, 90 Count Capsules. The recall was initiated in response to an FDA inspection that identified mislabeling issues. Specifically, the product named on the label is not the actual product contained in the bottle, and the ingredients listed on the label are not the actual ingredients contained in the product.
The affected product is identified by Lot # R1018 and UPC 0 65176 55958 5. The recall covers products distributed in California, Maryland, and New York. The FDA has classified this recall as Class III, indicating that the mislabeling is unlikely to cause adverse health consequences.
Consumers who have purchased this product should stop using it and return it to the place of purchase for a refund or contact the recalling firm for further instructions.
The recalled product
- 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***".
- Manufacturer
- Healthmaxx Global Inc.
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 5,223
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot # R1018 UPC 0 65176 55958 5
Distribution
Part of a larger recall action
This product is one of 28 recalled by Healthmaxx Global Inc. under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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