Good Herbs MPA Powder Recalled for GMP Violations
Good Herbs, Inc. is recalling MPA powder because it was not manufactured under Good Manufacturing Practices (GMPs).
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 II and involves a GMP violation without reported illnesses or specific high-risk pathogens, fitting the criteria for a moderate severity score.
Plain-English summary
Good Herbs, Inc. is recalling approximately 1,204 units of MPA powder. The recall was initiated because the products were not manufactured under Good Manufacturing Practices (GMPs).
The affected products were distributed nationally in Arizona, California, Connecticut, Florida, Indiana, Maine, Michigan, Missouri, Mississippi, North Carolina, New Hampshire, New York, Ohio, Oregon, Rhode Island, Texas, Virginia, and Wyoming. No international distribution was reported. All lots were distributed on or after October 17, 2013.
Consumers who have this product should stop using it and contact the recalling firm for further instructions.
The recalled product
- Product
- Good Herbs, Inc., MPA, powder, 550 Oliver Dr Troy, MI 48084 The Quality Herb That Works
- Manufacturer
- Good Herbs, Inc.
- Category
- Food — Herbal Supplements
- Hazard
- Affected units
- 1,204
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 (2)
- All Lots distributed on or after October 17
- 2013
Distribution
Part of a larger recall action
This product is one of 118 recalled by Good Herbs, 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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