Healthmaxx Global Recalls MAX Brand Resveratrol Capsules for Mislabeling
Healthmaxx Global Inc. is voluntarily recalling MAX Brand Resveratrol capsules because the label does not match the actual product or ingredients contained.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class III and involves mislabeling where the label does not match the contents. Per the rubric, minor labeling errors and Class III recalls are typically scored as 1 or 2; this is scored as 2 due to the discrepancy between labeled and actual ingredients.
Plain-English summary
Healthmaxx Global Inc. is voluntarily recalling 2,659 bottles of MAX Brand Resveratrol, 120 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, and the ingredients listed are not the actual ingredients contained.
The affected product is identified by Lot # A0830 and UPC 0 65176 30325 6. The recall covers distribution in California, Maryland, and New York. The FDA has classified this recall as Class III, indicating that use of the product is not likely to cause adverse health consequences.
Consumers who have purchased this product should stop using it and contact the recalling firm for further instructions or a refund.
The recalled product
- Product
- MAX Brand RESVERATROL, 120 Count Capsules. Product labeling reads in part:"MAX RESVERATROL***Dietary Supplement 120 CAPSULES***Manufactured in FDA Approved Facility for:HealthMax Products Inc. Altadena, CA 91001***0 65176 30325 6".
- Manufacturer
- Healthmaxx Global Inc.
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 2,659
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 # A0830 UPC 0 65176 30325 6
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.
See all 28 products in this recall →Related recalls
Same manufacturer · Healthmaxx Global Inc.
See all →- ModerateHealthmaxx Recalls Organic Grapeseed Extract Due to Mislabeling
FDA (Food) · 2013-10-02
- ModerateHealthmaxx Recalls MAX Organic Blueberry Capsules for Mislabeling
FDA (Food) · 2013-10-02
- ModerateHealthmaxx Recalls Stem Cell Enhance Supplements Due to Mislabeling
FDA (Food) · 2013-10-02
- LowHealthmaxx Global Recalls MAX Nitric Oxide Enhance Due to Mislabeling
FDA (Food) · 2013-10-02
- ModerateHealthmaxx Global Recalls Max Blood Sugar Defense Due to Mislabeling
FDA (Food) · 2013-10-02
Same hazard · mis labeling
See all →- ModerateMedline Trach Tube Kit Recalled for Component Labeling Discrepancy
FDA (Devices) · 2026-09-02
- ModerateAVID Medical Recalls Halyard Total Joint Kits for Latex Labeling Deficiency
FDA (Devices) · 2026-09-02
- ModerateOlympus Recalls PowerSeal Sealer Due to Incorrect Outer Box Labeling
FDA (Devices) · 2026-09-02
- HighSura Tanmen Ramen Noodles Recalled for Undeclared Fish Allergens
FDA (Food) · 2026-09-02
- SevereWhite Vein Advanced Alkaloids Chewable Tablets Recall for Excess Active Ingredient
FDA (Food) · 2026-09-02