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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 Assurance of Sterility; potential leakage from administrative port.

Agency Publication Date: January 24, 2014
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Affected Products

Product: Aminosyn 3.5% M Sulfite-Free, A Crystalline Amino Acid Solution* with Maintenance Electrolytes with Phosphorus, 1000 mL bag, Rx only. Hospira Inc, Lake Forest, IL, 60045. NDC: 0409-4196-05

Lot #: 26-123-JT, Exp: 8/14

Lot Numbers:
26-123-JT
Product: Heparin Sodium 2000 USP Heparin Units per 1000 mL (2 USP Heparin Units/mL) in 0.9% Sodium Chloride Injection, Rx only. Hospira, Lake Forest, IL 60045. NDC 0409-7620-59.

Lot #: 26-125-JT, Exp: 8/14

Lot Numbers:
26-125-JT

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 67317
Status: Resolved
Manufacturer: Hospira Inc.
Manufactured In: United States
Units Affected: 2 products (15258 bags; 27780 bags)

Were You Affected by This Recall?

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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.