Healthmaxx Recalls Hyper II Lecithin Softgels Due to Mislabeling
Healthmaxx Global Inc. is voluntarily recalling 817 bottles of Hyper II Lecithin softgels 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, which indicates the product is not likely to cause adverse health consequences. The hazard is limited to mislabeling, which fits the Moderate severity criteria for minor labeling errors.
Plain-English summary
Healthmaxx Global Inc. is voluntarily recalling 817 bottles of Hyper II LECITHIN, 100 Count Softgels. The recall was initiated in response to an FDA inspection. The product was distributed in California, Maryland, and New York.
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 has Lot # LIN0130 and UPC 6 65176 01115 3.
Consumers who have purchased this product should stop using it and contact the recalling firm for further instructions.
The recalled product
- Product
- Hyper II LECITHIN, 100 Count Softgels. Product labeling reads in part:"Hyper II LECITHIN***Dietary Supplement 100 Softgels***6 65176 01115 3***Manufactured for:HealthMax Products Co. Altadena, CA 91001***".
- Manufacturer
- Healthmaxx Global Inc.
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 817
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 # LIN0130 UPC 6 65176 01115 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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