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Becton Dickinson & Co. recalls BD PhoenixTM AP, Catalog Number 448010 The BD Phoenix" AP instrument is designed for use with the BD Phoenix" system is
Recalled December 13, 2017 · FDA recall Z-0198-2018 · Becton Dickinson &
Hazard
Potential unexpected movement of robot arm · FDA Class III
Units
7 units
Sold at
Worldwide Distribution - US including CA, NC & TN Internationally: Canada
Description
Potential unexpected movement of robot arm
Product
BD PhoenixTM AP, Catalog Number 448010 The BD Phoenix" AP instrument is designed for use with the BD Phoenix" system is intended to standardize ID broth tube inoculum, add AST indicator to the AST broth tube and transfer an aliquot of ID broth to AST broth tubes, as required for preparing samples for use on the BD Phoenix" system, which performs identification and susceptibility testing
Manufacturer(s)
Becton Dickinson & Co.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →