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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 Device

Bio-Rad Laboratories, Inc.: Bio-Rad received four customer complaints from 11/30/2022 to 12/21/2022 on BioPlex 2200 Anti-CCP Kit (Lot 301481) stating that results were discrepant while performing lot-to-lot validation against previous lots. Internal testing at Bio-Rad has demonstrated that Lot No. 301481 exhibits a specificity of 94.5% (95% CI 91.8  96.4) whereas the IFU indicates a specificity of 97.8% (95% CI 96.1  98.8%). The reduction in specificity may lead to an increase in the number of

Agency Publication Date: April 12, 2023
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Affected Products

Product: BioPlex 2200, Anti-CCP Reagent Pack, REF 665-3250, IVD

Lot # 301481; UDI GTIN: 00847865000857

Lot Numbers:
301481
Product: BioPlex 2200, Anti-CCP Calibrator Set, REF 663-3200, IVD

Lot # 53727; UDI GTIN: 00847865000819

Lot Numbers:
53727

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 91854
Status: Active
Manufacturer: Bio-Rad Laboratories, Inc.
Manufactured In: United States
Units Affected: 2 products (1544 units; 225 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.