Healthmaxx Recalls Organic OPC69 Dietary Supplements Due to Mislabeling
Healthmaxx Global Inc. is voluntarily recalling 3,816 bottles of MAX Brand Organic OPC69 dietary supplements because the label does not match the actual product 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, which aligns with the Moderate severity criteria for labeling errors.
Plain-English summary
Healthmaxx Global Inc. is voluntarily recalling 3,816 bottles of MAX Brand Organic OPC69, 300 Count Capsules. This recall was initiated 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 in the bottle, and the ingredients listed on the label are not the actual ingredients contained. The affected product is identified by Lot # OP0921 and UPC 0 65176 51257 3.
The product was distributed in California, Maryland, and New York. Consumers who have this product should stop using it and contact the recalling firm for further instructions.
The recalled product
- Product
- MAX Brand Organic OPC69, 300 Count Capsules Product labeling reads in part:"MAX ORGANIC OPC69 MAXIMUM STRENGTH***DIETARY SUPPLEMENT 300 Capsules***0 65176 51257 3***Manufactured in FDA Approved Facility for:HealthMax Products Inc. Altadena, CA 91001***".
- Manufacturer
- Healthmaxx Global Inc.
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 3,816
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 # OP0921 UPC 0 65176 51257 3
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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