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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

Baxter Healthcare Corp.: Cross Contamination w/Other Products Discoloration: A damaged manufacturing component may create a risk of batch to batch carryover between products and also some of the products may have discoloration.; Cross Contamination w/Other Products Discoloration: A damaged manufacturing component may create a risk of batch to batch carryover between products and also some of the products may have discoloration.

Agency Publication Date: December 29, 2010
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Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 56700
Status: Resolved
Manufacturer: Baxter Healthcare Corp.
Manufactured In: United States
Units Affected: 11 products (7,384 units; 16,472 units; 9,066 units; 8,814 units; 8,946 units; 16,474 units; 9,060 units; 47,130 units; 75,882 units; 13,752 units; 24,444 units)

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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.