Sundial Ethiopian Abish Fennugreek Seed Powder Recalled for Misbranding
Sundial Herbal Products is recalling Ethiopian Abish Fennugreek Seed Powder because it is misbranded and deemed an unapproved drug.
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 misbranding and unapproved drug claims without reported illnesses or injuries, fitting the criteria for moderate severity.
Plain-English summary
Sundial Herbal Products is recalling Sundial Ethiopian Abish (Fennugreek Seed Powder) under a permanent injunction. The product is distributed in New York and was manufactured, processed, packed, held, and/or distributed between January 1, 2014, and May 27, 2020.
The recall is required because the products are misbranded and deemed unapproved drugs based on their labeling claims. The source text does not report any specific illnesses, injuries, or deaths associated with this recall.
Consumers should stop using the product and follow instructions provided by the recalling firm or the FDA regarding disposal or return.
The recalled product
- Product
- "SUNDIAL***ETHIOPIAN ABISH (FENNUGREEK SEED POWDER.)***"
- Manufacturer
- Sundial Herbal Products
- Category
- Food — Herbal Supplements
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 (5)
- Product manufactured
- processed
- packed
- held
- and/or distributed during the time period beginning 1/1/2014 through 5/27/2020.
Distribution
Distributed in 1 state:
Part of a larger recall action
This product is one of 68 recalled by Sundial Herbal Products 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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