Healthmaxx Global Recalls Max Probiotic Tablets Due to Mislabeling
Healthmaxx Global Inc. is voluntarily recalling Max Probiotic-90 tablets because the product label does not match the actual ingredients or product contained.
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 where the label does not match the contents, which aligns with the rubric for moderate severity.
Plain-English summary
Healthmaxx Global Inc. has initiated a voluntary recall of Max Probiotic-90 tablets, a dietary supplement manufactured for HealthMax Products Inc. The recall was initiated in response to an FDA inspection that identified mislabeling issues.
The specific problems identified are that the product named on the label is not the actual product contained, and the ingredients listed on the label are not the actual ingredients contained in the product. The affected product is identified by Lot# PMG 0922 and UPC 6 65176 30625 9.
The product was distributed 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 Probiotic-90 tablets UPC 6 65176 30625 9***Dietary Supplement Product labeling reads in part:"*DIETARY SUPPLEMENT***Manufactured for:HealthMax Products Inc. Altadena, CA 91001
- Manufacturer
- Healthmaxx Global Inc.
- Category
- Food — Dietary Supplement
- Hazard
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# PMG 0922
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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