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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

Carlsbad Technology Inc: Presence of Undeclared Color Additive; product capsule shells contain undeclared FD&C Yellow #5 and discrepancies between labeled inactive ingredients in the package inserts and the inactive ingredients contained in the products; Presence of Undeclared Color Additive; product capsule shells contain undeclared FD&C Yellow #5 and Discrepancies between labeled inactive ingredients in the package inserts and the inactive ingredients contained in the products; Some product ca

Agency Publication Date: September 28, 2007
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Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 38619
Status: Resolved
Manufacturer: Carlsbad Technology Inc
Manufactured In: United States
Units Affected: 3 products (3,628 bottles; PCC9eS001 - 3,270 capsules, PCC9eS002 - 3,432 capsules; PCC10eS001- 6,971 bottles, PCC10eS002 - 6,760 capsules, PCC10eS003 - 6,475 capsules)

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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.