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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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Critical RiskFDA Device

Baxter Healthcare Corp: Particulate matter found inside the fluid path.

Agency Publication Date: October 31, 2014
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Affected Products

Product: Baxter 2B8011 Empty INTRA VIA Container with PVC Ports, Sterile fluid path, 150 ml, Admixture Products and Accessories. The lntraVia Empty Plastic Container is intended for use in the preparation and administration of drug admixtures.

Product code: 2B8011 Lot Number: UR13D15112

Lot Numbers:
2B8011
Number
Product: Baxter 2B8013 Empty INTRA VIA Container with PVC Ports (Sterile, nonpyrogenic fluid path) ,500 ml. Admixture Products and Accessories The lntraVia Empty Plastic Container is intended for use in the preparation and administration of drug admixtures.

Product code 2B8013 Lot Number: UR13K14095

Lot Numbers:
2B8013
Number

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 69181
Status: Resolved
Manufacturer: Baxter Healthcare Corp
Manufactured In: United States
Units Affected: 2 products (94,224; 20448)

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.