FDAFDA · Food and drugs·Recall number Z-0198-2018
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
Published December 13, 2017 · Recall initiated: June 1, 2017
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Potential unexpected movement of robot arm
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Becton Dickinson & Co.
- Distributor
- Worldwide Distribution - US including CA, NC & TN Internationally: Canada
- Lot
- Serial Numbers: AP0447, AP0448, AP0449, AP0450, AP0451, AP0458 & AP0463.
- Risk classification
- Class III
- Area (FDA)
- device
- Country
- United States
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