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Ortho-Clinical Diagnostics recalls VITROS 5600 Integrated System, Version 3.3.1 & below For use in the in vitro quantitative, semi-quantitative, and qu

Recalled December 26, 2018 · FDA recall Z-0650-2019 · Ortho-Clinical Diagnostics

Hazard
Software anomaly may incorrectly extend the on-analyzer stability time for a loaded VITROS Reagent. · FDA Class II
Units
2413
Sold at
US Nationwide Distribution

Description

Software anomaly may incorrectly extend the on-analyzer stability time for a loaded VITROS Reagent.

Product
VITROS 5600 Integrated System, Version 3.3.1 & below For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Chemistry Product Slides, VITROS Chemistry Products MicroTip Reagents and VITROS Immunodiagnostic Products Reagents.
Manufacturer(s)
Ortho-Clinical Diagnostics

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Ortho-Clinical Diagnostics recalls VITROS 5600 Integrated System, Version 3.3.1 & below For use in the in vitro quantitative, semi-quantitative, and qu | RecallWatchUSA