Sundial Herbal Diabetics Formula Recalled for Misbranding and Unapproved Drug Status
Sundial Herbal Products is recalling its Traditional Herbal Formula for Diabetics because the product is misbranded and considered 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 status without reported illnesses or injuries, fitting the criteria for moderate severity.
Plain-English summary
Sundial Herbal Products is recalling "SUNDIAL***TRADITIONAL HERBAL FORMULA***DIABETICS***" packaged in boxes. The recall is required by an Order of Permanent Injunction. The product was distributed in New York.
The FDA has determined that the products are misbranded and deemed unapproved drugs based on their labeling claims. The recall covers product manufactured, processed, packed, held, and/or distributed between January 1, 2014, and May 27, 2020.
Consumers who have this product should stop using it and contact the recalling firm for further instructions.
The recalled product
- Product
- "SUNDIAL***TRADITIONAL HERBAL FORMULA***DIABETICS***" packaged in boxes
- Manufacturer
- Sundial Herbal Products
- Category
- Drug — Herbal Supplement
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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