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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

Unico Holdings, Inc.: Unico Holdings is recalling over the counter (OTC) oral sodium phosphate (OSP) products sold under various brand names. This recall is being initiated in response to an FDA advisory issued on December 11, 2008 stating that OTC OSP products are not recommended for bowel cleansing, due to the rare risk of acute kidney injury from the use of OSP products with the dosages used for bowel cleansing. A

Agency Publication Date: December 30, 2008
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Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 50566
Status: Resolved
Manufacturer: Unico Holdings, Inc.
Manufactured In: United States
Units Affected: 14 products (27,228 kits; 11,256 kits; 10,698 kits; 840 kits; 3,828 kits; 4,626 kits; 1,440 kits; 1,860 kits; 85,662 kits; 3,672 kits; 360 kits; 1,416 kits; 840 kits; 80,580 kits)

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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.