BD Phoenix™ NMIC-300 448871Recalls & reported problems
Becton, Dickinson And Company · Panel Phoenix Nmic 300 · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 30382904488711), received between Oct 15, 2019 and Oct 15, 2019 — classified as 1 injury.
The most frequently reported specific device problem is “Incorrect, Inadequate or Imprecise Result or Readings” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Incorrect, Inadequate or Imprecise Result or Readings1
Patient problems
- Test Result1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryOct 15, 2019Incorrect, Inadequate or Imprecise Result or Readings
THE CUSTOMER REPORTED A DISCREPANT RESULT WHILE USING THE BD PHOENIX¿ NMIC PANEL. THE PANEL RESULT WAS 8/4 (S) TO AMP/SULBACTAM FOR ACINETOBACTER BAUMANII. THE TECH FORGOT THAT THE AMP/SULBACTAM WAS ON THE PANEL AND A KB WAS SET UP. THE KB RESULT WAS INTERMEDIATE. THE NMIC-300 PANEL WAS REPEATED SINCE THERE WAS DISCREPANCY BETWEEN THE PHOENIX PANEL AND THE K/B. THE REPEAT PHOENIX RESULT WAS >16/8 (R). THE PATIENT WAS SENT HOME ON AMP/SULBACTAM SINCE IT WAS ORIGINALLY REPORTED AS SUSCEPTIBLE. THE CUSTOMER IS UNABLE TO PROVIDE ANY ADDITIONAL INFORMATION.
Patient problems: Test Result
MAUDE report 9193644 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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