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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Drug

Standard Homeopathic Company, Inc.: Blend Uniformity:Standard Homeopathic Company initiated the recall due to an FDA investigation of its manufacturing facility. The company, in working with the FDA, has identified manufacturing processes of Teething Tablets that can be improved to ensure uniformity in dosage. In addition, adverse events have been reported for the affected product but the FDA has said that a conclusive link to Teeth; Blend Uniformity: Standard Homeopathic Company initiated the r

Agency Publication Date: February 9, 2011
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Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 57067
Status: Resolved
Manufacturer: Standard Homeopathic Company, Inc.
Manufactured In: United States
Units Affected: 6 products (5,703,606 Bottles; 673,720 Bottles; 252,266 Bottles; 153,322 Bottles; 78 packs (pack = 6 retail units x 125 tablet bottles); 221,751 Packets)

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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 · 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.