medical Class II Updated 2024-10-02

Becton Dickinson & Co. recalls BD Phoenix 100-Intended for the rapid identification (ID) an

Recalled Product

BD Phoenix 100-Intended for the rapid identification (ID) and antimicrobial susceptibility testing (AST) of clinically significant bacteria. The BD Phoenix System provides rapid results for most aerobic and facultative anaerobic Grampositive bacteria. Catalog Number: 448100


Hazard / Issue

Escherichia coli (E. coli) misidentification for clinical samples that were tested on BD Phoenix" M50 instrument and BD Phoenix" 100, may lead to misdiagnosis and inappropriate treatment of infections caused by E. coli,

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: UDI: 00382904481001 All serial numbers
View official government recall

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