Dark with Browned Ghee is wrapped in a foil and jacketed with black paper. There is a white sticker on the front that says Sanity Chocolate. On the back label there is the batch name listed above, address listed above and ingredient list. Average net weight is 0.75 oz. There is no UPC code. The label is read in parts: "***Dark - w/browned Ghee***Ingredients: Organic cacao, organic sugar, browned Ghee*** Processed in a facility that also handles nuts gluten and dairy ***1280 E Main St Cottage Grove, OR ***".
Class I - DangerousWhat Should You Do?
- Check if you have this product: None
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- SANITY CHOCOLATE
- Reason for Recall:
- Label declares ghee, but it does not declare milk.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Dark with Browned Ghee is wrapped in a foil and jacketed with black paper. There is a white sticker on the front that says Sanity Chocolate. On the back label there is the batch name listed above, address listed above and ingredient list. Average net weight is 0.75 oz. There is no UPC code. The label is read in parts: "***Dark - w/browned Ghee***Ingredients: Organic cacao, organic sugar, browned Ghee*** Processed in a facility that also handles nuts gluten and dairy ***1280 E Main St Cottage Grove, OR ***".
Product Codes/Lot Numbers:
None
Distribution:
Distributed in: OR
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: F-0500-2020
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