Healthmaxx Recalls Stem Cell Enhance Supplements Due to Mislabeling
Healthmaxx Global Inc. is voluntarily recalling MAX Brand Stem Cell Enhance dietary supplements because the product label does not match the actual contents or ingredients.
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, which indicates the product is unlikely to cause adverse health consequences. The hazard is limited to mislabeling of ingredients and product identity, fitting the criteria for minor labeling errors.
Plain-English summary
Healthmaxx Global Inc. has initiated a voluntary recall of MAX Brand Stem Cell Enhance, 1.0 fl. oz. dietary supplements. The recall was initiated in response to a U.S. Food and Drug Administration (FDA) inspection that identified mislabeling issues.
The FDA determined that 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 # SC0516 with an expiration date of December 2016. There is no UPC code listed for the product.
The recall involves 31,259 bottles distributed in California, Maryland, and New York. Consumers who purchased this product should stop using it and contact the recalling firm for further instructions.
The recalled product
- Product
- MAX Brand Stem Cell Enhance, 1.0 fl. oz. Product labeling reads in part:"MAX Stem Cell Enhance***1.0fl. oz(30ml)***".
- Manufacturer
- Healthmaxx Global Inc.
- Category
- Food — Dietary Supplements
- Hazard
- Affected units
- 31,259
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 # SC0516 Exp. Date: Dec 2016 No UPC Code
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
- 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
- ModerateHealthmaxx Global Recalls MAX Brand Proste-Support Tablets 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