Healthmaxx Global Recalls MAX Brand LIVERAID Dietary Supplement for Mislabeling
Healthmaxx Global Inc. is voluntarily recalling MAX Brand LIVERAID dietary supplements because the product and ingredient labels do not match the actual contents.
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 minor labeling errors without reported illnesses or injuries, fitting the criteria for a moderate severity score.
Plain-English summary
Healthmaxx Global Inc. is voluntarily recalling 3,197 bottles of MAX Brand LIVERAID, 200 Count Bottle, in response to a U.S. Food and Drug Administration (FDA) inspection. The recall is due to mislabeling issues where 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 # L0126 and UPC 6 65176 35168 6. The recall covers distribution in California, Maryland, and New York.
Consumers who have purchased this product should stop using it and contact the recalling firm for further instructions.
The recalled product
- 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***".
- Manufacturer
- Healthmaxx Global Inc.
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 3,197
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 # L0126 UPC 6 65176 35168 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