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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

Hospira Inc.: Lack of Efficacy; the affected lot was initially received in a frozen state. The labeling claim for these products does not support their use when frozen.; Lack of Efficacy; affected lots were initially received in a frozen state. The labeling claim for these products does not support their use when frozen.; Lack of Efficacy; the affected lots were initially received in a frozen state. The labeling claim for these products does not support their use when frozen.; Lack of Efficac

Agency Publication Date: March 1, 2006
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Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 34501
Status: Active
Manufacturer: Hospira Inc.
Manufactured In: United States
Units Affected: 8 products (200 vials; 100 - 20 mL vials and 50 - 50 mL vials; 40 cartons; 50 vials; 600 cartons; 900 units; 100 cartons; 200 cartons)

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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.