Healthmaxx Global Recalls MAX Brand CoQ10 Capsules Due to Mislabeling
Healthmaxx Global Inc. is voluntarily recalling MAX Brand CoQ10 capsules 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 2/5 (Moderate).
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, FDA Class III recalls are typically scored 1 or 2, and this is a voluntary precautionary recall for labeling errors.
Plain-English summary
Healthmaxx Global Inc. is voluntarily recalling 6,126 bottles of MAX Brand CoQ10, 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 do not match the actual ingredients contained.
The affected product is identified by Lot # H0411 and UPC 6 65176 30162 9. The bottles were distributed in California, Maryland, and New York. The product was manufactured in an FDA-approved facility for HealthMax Products Co. in Altadena, CA.
Consumers who have this product should stop using it and contact Healthmaxx Global Inc. for further instructions. This recall is classified as Class III by the FDA, indicating that the mislabeling is unlikely to cause adverse health consequences.
The recalled product
- Product
- MAX Brand CoQ10, 90 Count Capsules Product labeling reads in part:"MAX CoQ10***DIETARY SUPPLEMENT 90 Capsules***6 65176 30162 9***Manufactured in FDA Approved Facility for:HealthMax Products Co. Altadena, CA 91001***".
- Manufacturer
- Healthmaxx Global Inc.
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 6,126
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 # H0411 UPC 6 65176 30162 9
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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