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
Reported: December 13, 2017 Initiated: June 1, 2017 #Z-0198-2018
Product Description
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
Reason for Recall
Potential unexpected movement of robot arm
Details
- Recalling Firm
- Becton Dickinson & Co.
- Units Affected
- 7 units
- Distribution
- Worldwide Distribution - US including CA, NC & TN Internationally: Canada
- Location
- Sparks, MD
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Becton Dickinson & Co.. Units affected: 7 units.
Why was this product recalled? ▼
Potential unexpected movement of robot arm
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 13, 2017. Severity: Low. Recall number: Z-0198-2018.
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