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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

Ortho-Clinical Diagnostics: Potential for biased results when a Multiple Window (MW) code is associated with results generated by the VITROS 4600 Chemistry System, the VITROS 5600 Integrated System and the VITROS 5,1 Chemistry System. MW codes may be associated with results from any of the following VITROS Chemistry Products using multiple point (multipoint) rate measurements. The MicroSlide assays that could be affected

Agency Publication Date: June 9, 2014
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Affected Products

Product: VITROS 4600 Chemistry System, Product Code/Catalog Number 6802445 for in vitro diagnostic use.

Software Version 3.0 and lower; Serial Numbers J46000108 through J46000403

Product: VITROS 5600 Integrated System, Product Code/Catalog Number 6802413 for in vitro diagnostic use.

Software Version 3.0 and lower; Serial Numbers J56000110 through J56001912

Product: VITROS 5,1 FS Chemistry System and VITROS 5,1 FS Refurbished, Product Codes/Catalog Numbers 6801375, 6801890 for in vitro diagnostic use.

Software Version 2.7 and below; VITROS 5,1 FS Chemistry System Serial Numbers: J34000102 through J34002323; VITROS 5,1 FS Chemistry System Refurbished Serial Numbers: ¿34000337, ¿34001840, ¿34000316, ¿34001389, 34001317, ¿34000538, ¿34000552, ¿34000360, ¿34000451, ¿34000833, ¿ 34001572, ¿34000193, ¿34001633, ¿34000851, ¿34001345, ¿34001396, 34001809, ¿34001897, ¿34001240, ¿34001612, ¿34001311, ¿34000212, 34001472, ¿34001172, ¿34001390, ¿34000557, ¿34000893, ¿34001297, 34001378, ¿34001218, ¿34000318, ¿34000596, ¿34000497, ¿34000495, 34000529, ¿34000478, ¿34001569, ¿34001243, ¿34001504, ¿34000947, 34001422, ¿34000805, ¿34000631, ¿34001248, ¿34001251, ¿34000601, 34001274, ¿34001668, ¿34001850, ¿34001379, ¿34000133, ¿34000642, 34001626.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 68271
Status: Resolved
Manufacturer: Ortho-Clinical Diagnostics
Manufactured In: United States
Units Affected: 3 products (Domestic - 82, Foreign - 213 units; Domestic - 835 units, Foreign - 921 units; Domestic - 597 units, Foreign - 1381 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.