Diva Fam Inc. is recalling approximately 5.4 million units of various Sea Moss Gel Superfood products because they may be contaminated with Clostridium botulinum. The recall affects 14 different flavors sold in 16-ounce glass jars across the United States. These products were sold nationwide through 31 different retail customers and directly to consumers via online sales.
The product may contain Clostridium botulinum, which can cause botulism, a rare but serious and potentially fatal form of food poisoning. Botulism can cause symptoms such as general weakness, dizziness, double vision, and trouble speaking or swallowing, and can lead to paralysis of the breathing muscles.
You have 2 options:
Glass jar sold individually.
Glass jar sold individually.
Glass jar sold individually.
Glass jar sold individually.
Glass jar sold individually.
Glass jar sold individually.
Glass jar sold individually.
Glass jar sold individually.
Glass jar sold individually.
Glass jar sold individually.
Glass jar sold individually.
Glass jar sold individually.
Glass jar sold individually.
Glass jar sold individually.
“True Sea Moss, jar lid label”
“True Sea Moss Sea Moss Gel Superfood, jar label (multiple flavors)”
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 · 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.