Je Dois Lavoir LLC is recalling 783 bottles of 365 SKINNY High Intensity Capsules (600 mg, 30-count). Testing found the product contains sibutramine, an undeclared drug ingredient that was previously removed from the U.S. market due to safety concerns. These capsules were sold online through the manufacturer's website to consumers throughout the United States and Canada.
Sibutramine can significantly increase blood pressure and heart rate, posing a serious risk to individuals with a history of heart disease, heart failure, or stroke. No injuries or illnesses have been reported to date in connection with this recall.
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Recall #: D-0631-2022
Photo 1 – Labeling, 365 Skinny, High Intensity
Photo 2 – Labeling, 365 Skinny, Emergency Boutique
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES · FDA Press Release (1) · FDA Press Release (2) · Raw API Response
openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.