Good Herbs Bee Formula Recalled for GMP Violations
Good Herbs, Inc. is recalling Bee Formula bottles because they were not manufactured under Good Manufacturing Practices (GMPs).
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall is classified as FDA Class II. Per the rubric, FDA Class II recalls without specific reports of hospitalization or injury are assigned a score of 3 (High).
Plain-English summary
Good Herbs, Inc. is voluntarily recalling approximately 1,099 units of Bee Formula, available in 1 and 4 oz bottles. The product was distributed nationally to Arizona, California, Connecticut, Florida, Indiana, Maine, Michigan, Missouri, Mississippi, North Carolina, New Hampshire, New York, Ohio, Oregon, Rhode Island, Texas, Virginia, and Wyoming. All lots were distributed on or after October 17, 2013.
The recall was initiated because the products were not manufactured under Good Manufacturing Practices (GMPs). The FDA has classified this recall as Class II, indicating a situation that may cause temporary or medically reversible adverse health consequences.
Consumers who purchased this product should stop using it and contact the recalling firm for further instructions or a refund.
The recalled product
- Product
- Good Herbs, Inc., BEE FORMULA, 1 & 4 oz bottle, 550 Oliver Dr Troy, MI 48084 The Quality Herb That Works
- Manufacturer
- Good Herbs, Inc.
- Category
- Food — Herbal Supplements
- Hazard
- Affected units
- 1,099
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 117 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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