The Recall Desk
ModerateFDA (Food)·F-0176-2015·Announced 2014-11-05

Good Herbs Digestive Kit Recalled for GMP Violations

Good Herbs, Inc. is recalling its Digestive Kit 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 typically indicates a temporary or medically reversible health risk. The source text does not report any illnesses or injuries, and the hazard is a GMP violation rather than a specific pathogen or allergen, fitting the criteria for a moderate severity score.

Plain-English summary

Good Herbs, Inc. is recalling its Digestive Kit, a product manufactured in Troy, Michigan. The recall was initiated because the products were not manufactured under Good Manufacturing Practices (GMPs). Approximately 1,099 total units were 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 source text does not report any illnesses or injuries associated with this recall. Consumers who possess this product should stop using it and contact the recalling firm for further instructions.

The recalled product

Product
Good Herbs, Inc., DIGESTIVE KIT, kit, 550 Oliver Dr Troy, MI 48084 The Quality Herb That Works
Manufacturer
Good Herbs, Inc.
Category
Food — Dietary 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

Distributed in 18 states:

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.

See all 117 products in this recall →

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Same hazard · gmp violation

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