Good Herbs Yohimbe Recalled for Failure to Meet GMP Standards
Good Herbs, Inc. is recalling Yohimbe 1 oz bottles because the products were 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, which corresponds to a moderate severity score. The hazard is a failure to meet GMP standards, which is a regulatory compliance issue rather than a specific reported injury or high-risk pathogen.
Plain-English summary
Good Herbs, Inc. is voluntarily recalling approximately 1,204 units of Yohimbe, 1 oz bottles. The recall was initiated because the products were not manufactured under Good Manufacturing Practices (GMPs). The affected products are identified by the description "The Quality Herb That Works" and were distributed on or after October 17, 2013.
The recall covers distribution in the following states: AZ, CA, CT, FL, IN, ME, MI, MO, MS, NC, NH, NY, OH, OR, RI, TX, VA, and WY. No international distribution was reported.
Consumers who have purchased this product should stop using it and contact Good Herbs, Inc. for further instructions or a refund.
The recalled product
- Product
- Good Herbs, Inc., YOHIMBE, 1 oz bottle, 550 Oliver Dr Troy, MI 48084 The Quality Herb That Works
- Manufacturer
- Good Herbs, Inc.
- Category
- Food — Dietary Supplement
- 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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