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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

L. Perrigo Co.: Some dosing cups packaged with product lack the 1/2 teaspoon mark for dosing children 2 to 6 yrs of age.; Some dosing cups packaged with product lack the 1/2 teaspoon mark for dosing children 2 to 6 yrs of age which could result in administration of twice the recommended dose of dextromethorphan.

Agency Publication Date: November 1, 2007
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Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 44836
Status: Resolved
Manufacturer: L. Perrigo Co.
Manufactured In: United States
Units Affected: 6 products (864 bottles; 11,184 bottles; 51,120 bottles; 4,416 bottles; 2,040 bottles; 10,848 bottles)

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.