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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

Healthfirst Corp: Incorrect product insert distributed with kit; Products are mislabled with the incorrect manufacturer's package inserts - Warrick brand distributed with ProAir package insert.

Agency Publication Date: May 9, 2008
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Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 38285
Status: Resolved
Manufacturer: Healthfirst Corp
Manufactured In: United States
Units Affected: 2 products (15,068 HM Kits; 4,659 SM Kits; and 879 BD Kits for a total of 20,606 Kits.; 96 HM Kits; and 105 SM Kits for a total of 201 Kits.)

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.