FDAAugust 1, 2024device

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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,

What to do

FDA enforcement status: Ongoing

Brands named

becton dickinsonbectonbecton dickinson

UPCs

00382904481001

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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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 — Recall Details · AllClear