BD Phoenix™ NID 448007Recalls & reported problems
Becton, Dickinson And Company · BD Phoenix™ NID · Class 1
Quick summary
This BD Phoenix NID panel, used to identify gram-negative bacteria, has 133 reports, most describing incorrect, inadequate or imprecise results. The reports mention 1 injury and no deaths, and no recalls name this device. Reports rose to 42 in the last 12 months from 16 in the previous 12.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 138
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 138 adverse event reports that list this exact device (DI 00382904480073), received between Mar 27, 2021 and Sep 29, 2026 — classified as 1 injury, 137 malfunctions.
The most frequently reported specific device problem is “Incorrect, Inadequate or Imprecise Result or Readings” (135 reports).
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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Incorrect, Inadequate or Imprecise Result or Readings135
- False Positive Result2
- Incorrect Measurement1
Patient problems
- No Clinical Signs, Symptoms or Conditions138
Recent adverse event reports
The 25 most recent of 138 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50941221 ↗MalfunctionSep 29, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50938975 ↗MalfunctionSep 17, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50809420 ↗MalfunctionSep 15, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50776507 ↗MalfunctionSep 15, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50776502 ↗MalfunctionSep 15, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50773772 ↗MalfunctionAug 28, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50503524 ↗MalfunctionAug 28, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50497115 ↗MalfunctionAug 26, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50460946 ↗MalfunctionAug 26, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50456696 ↗MalfunctionAug 24, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50408867 ↗MalfunctionAug 21, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50379905 ↗MalfunctionAug 21, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50379899 ↗MalfunctionAug 12, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50220930 ↗MalfunctionAug 11, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50214126 ↗MalfunctionAug 11, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50213121 ↗MalfunctionAug 11, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50207425 ↗MalfunctionJul 30, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50084464 ↗MalfunctionMay 27, 2026Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED WHILE USING THE BD PHOENIX¿ NID A PATIENT URINE ISOLATE (ESCHERICHIA COLI) WAS MISIDENTIFIED AS PASTEURELLA AEROGENES. THE USER VERIFIED THE FINAL RESULT USING MALDI. NO HEALTH IMPACT OR CONSEQUENCE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25300815 ↗MalfunctionMay 26, 2026Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED WHILE USING THE BD PHOENIX¿ NID A PATIENT ISOLATE (SERRATIA LIQUEFACIENS) WAS MISIDENTIFIED AS SERRATIA PLYMUTHICA. THE USER VERIFIED THE FINAL RESULT USING MALDI. NO HEALTH IMPACT OR CONSEQUENCE REPORTED. THIS IS REPORT 2 OF 2.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25278705 ↗MalfunctionMay 26, 2026Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED WHILE USING THE BD PHOENIX¿ NID A PATIENT ISOLATE (SERRATIA LIQUEFACIENS) WAS MISIDENTIFIED AS SERRATIA PLYMUTHICA. THE USER VERIFIED THE FINAL RESULT USING MALDI. NO HEALTH IMPACT OR CONSEQUENCE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25277000 ↗MalfunctionMay 21, 2026Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED WHILE USING THE BD PHOENIX¿ NID A PATIENT ISOLATE (ESCHERICHIA COLI) WAS MISIDENTIFIED AS CITROBACTER KOSERI AND CITROBACTER FARMERI WHEN REPEAT TESTING WAS PERFORMED WITH AN AFFILIATED LABORATORY. NO INFORMATION COULD BE PROVIDED ON PATIENT IMPACT, BUT THE USER STATED THAT THE COLONY MORPHOLOGY WAS SIMILAR TO ESCHERICHIA COLI. THIS IS REPORT 2 OF 2.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25242695 ↗MalfunctionMay 21, 2026Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED WHILE USING THE BD PHOENIX¿ NID A PATIENT ISOLATE (ESCHERICHIA COLI) WAS MISIDENTIFIED AS CITROBACTER KOSERI AND CITROBACTER FARMERI WHEN REPEAT TESTING WAS PERFORMED WITH AN AFFILIATED LABORATORY. NO INFORMATION COULD BE PROVIDED ON PATIENT IMPACT, BUT THE USER STATED THAT THE COLONY MORPHOLOGY WAS SIMILAR TO ESCHERICHIA COLI.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25240705 ↗MalfunctionApr 30, 2026Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED WHILE USING THE BD PHOENIX¿ NID A PATIENT ISOLATE (ACINETOBACTER BAUMANNII) WAS MISIDENTIFIED AS MORAXELLA (FORMERLY BRANHAMELLA) CATARRHALIS. THE USER VERIFIED THE FINAL RESULT USING BACTERIAL CULTURE. NO HEALTH IMPACT OR CONSEQUENCE REPORTED. THIS IS REPORT 16 OF 17.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25051159 ↗MalfunctionApr 30, 2026Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED WHILE USING THE BD PHOENIX¿ NID A PATIENT ISOLATE (ACINETOBACTER BAUMANNII) WAS MISIDENTIFIED AS MORAXELLA (FORMERLY BRANHAMELLA) CATARRHALIS. THE USER VERIFIED THE FINAL RESULT USING BACTERIAL CULTURE. NO HEALTH IMPACT OR CONSEQUENCE REPORTED. THIS IS REPORT 17 OF 17.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25051145 ↗
Other GRAM NEGATIVE IDENTIFICATION PANEL devices
- VITEK® 2 GNBiomerieux , Inc. · Gram negative identification panel1 recall144 reports
- BD BBL™ Crystal™ E/NF 245000Becton, Dickinson And Company · GRAM NEGATIVE IDENTIFICATION PANEL1 report
- MicroScan B1010-41ABeckman Coulter, Inc. · Gram Negative Identification Panel1 report
- MicroScan B1017-411Beckman Coulter, Inc. · Gram Negative Identification Panel1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.