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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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Low RiskFDA Drug

Contact Pharmacal Corp.: No testing was performed for hyoscyamine sulfate and atropine sulfate ingredients in these products to determine satisfactory conformance to specifications and to verify stability of these products over labeled shelf life.

Agency Publication Date: September 12, 2006
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Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 36003
Status: Resolved
Manufacturer: Contact Pharmacal Corp.
Manufactured In: United States
Units Affected: 4 products (5,874/90-tablet bottles; 9,598 100-tablet bottles; 27,709/90-tablet bottles; 20,016 displays (12 x 2 tablets))

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.