BD Phoenix™ PMIC/ID-107 448607Recalls & reported problems
Becton, Dickinson And Company · Panel Phoenix Pmic/Id 107 · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
Quick summary
This BD Phoenix PMIC/ID-107 test panel has 169 reports, with no deaths and 2 injuries. Reports mostly describe bacteria being misidentified, such as Staphylococcus aureus reported as group B strep, and none list a patient symptom. The panel has 2 recalls: an open one for a minocycline formulation that can produce false resistance results, and a closed one for false resistance results with an antibiotic test. Reports fell from 75 in the prior 12 months to 11 in the latest 12 months.
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
- 169
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 2
Summary
The FDA's MAUDE database contains 169 adverse event reports that list this exact device (DI 30382904486076), received between Jul 2, 2021 and Mar 19, 2026 — classified as 2 injuries, 167 malfunctions.
The most frequently reported specific device problem is “Incorrect, Inadequate or Imprecise Result or Readings” (164 reports).
2 FDA recall records name this device's identifier, 1 still open.
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.
Reports received per month
Recalls naming this device
- Oct 13, 2022Class IIOpen, Classified
Misformulated minocycline-can cause erroneously increased Minimal Inhibitory Concentration (MIC) values when performing antibiotic susceptibility testing (AST) against minocycline and result in the reporting of false resistance for clinical samples if the initial Quality Control (QC) testing of the panel batch passes, delaying treatment of the patient with the most appropriate antibiotic
Z-0232-2023 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Dec 8, 2020Class IITerminated
BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant SXT result with S. aureus could lead to a potential loss of access to a preferred antibiotic regimen and potential reduction in effectiveness of treatment of the infection
Z-0760-2021 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Most reported problems
Device problems
- Incorrect, Inadequate or Imprecise Result or Readings164
- Device Markings/Labelling Problem2
- Incorrect Measurement2
- Device Ingredient or Reagent Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions169
Recent adverse event reports
The 25 most recent of 169 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 19, 2026Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED WHILE USING THE BD PHOENIX¿ PMIC/ID-107 A PATIENT ISOLATE (STAPHYLOCOCCUS EPIDERMIDIS) WAS MISIDENTIFIED AS STAPHYLOCOCCUS HAEMOLYTICUS. THE USER STATED, "THAT HE BELIEVES THAT THE PURITY PLATE WAS MIXED, AND CONSIDERS THIS TO BE A TECH ERROR, NOT A TRUE MISIDENTIFICATION." NO HEALTH IMPACT OR CONSEQUENCE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24639599 ↗MalfunctionMar 16, 2026Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED WHILE USING THE BD PHOENIX¿ PMIC/ID-107 A PATIENT ISOLATE (STAPHYLOCOCCUS SAPROPHYTICUS) WAS MISIDENTIFIED AS STAPHYLOCOCCUS AUREUS. THE USER VERIFIED THE FINAL RESULT USING REPEAT TESTING. NO HEALTH IMPACT OR CONSEQUENCE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24607726 ↗MalfunctionFeb 2, 2026Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED WHILE USING THE BD PHOENIX¿ PMIC/ID-107 A PATIENT ISOLATE (STAPHYLOCOCCUS AUREUS) WAS MISIDENTIFIED AS GROUP B STREP (GBS) OR STREPTOCOCCUS AGALACTIAE. THE USER VERIFIED THE FINAL RESULT USING CATALASE AND COAGULASE. THE USER ALSO NOTED PERFORMING REPEAT TESTING AND THAT THE ISOLATE WAS COAGULASE POSITIVE AND BETA HEMOLYTIC. NO HEALTH IMPACT OR CONSEQUENCE REPORTED. THIS IS REPORT 3 OF 4.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24236301 ↗MalfunctionFeb 2, 2026Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED WHILE USING THE BD PHOENIX¿ PMIC/ID-107 A PATIENT ISOLATE (STAPHYLOCOCCUS AUREUS) WAS MISIDENTIFIED AS GROUP B STREP (GBS) OR STREPTOCOCCUS AGALACTIAE. THE USER VERIFIED THE FINAL RESULT USING CATALASE AND COAGULASE. THE USER ALSO NOTED PERFORMING REPEAT TESTING AND THAT THE ISOLATE WAS COAGULASE POSITIVE AND BETA HEMOLYTIC. NO HEALTH IMPACT OR CONSEQUENCE REPORTED. THIS IS REPORT 4 OF 4.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24236299 ↗MalfunctionFeb 2, 2026Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED WHILE USING THE BD PHOENIX¿ PMIC/ID-107 A PATIENT ISOLATE (STAPHYLOCOCCUS AUREUS) WAS MISIDENTIFIED AS GROUP B STREP (GBS) OR STREPTOCOCCUS AGALACTIAE. THE USER VERIFIED THE FINAL RESULT USING CATALASE AND COAGULASE. THE USER ALSO NOTED PERFORMING REPEAT TESTING AND THAT THE ISOLATE WAS COAGULASE POSITIVE AND BETA HEMOLYTIC. NO HEALTH IMPACT OR CONSEQUENCE REPORTED. THIS IS REPORT 2 OF 4.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24236298 ↗MalfunctionJan 13, 2026Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED WHILE USING THE BD PHOENIX¿ PMIC/ID-107 A PATIENT ISOLATE (STAPHYLOCOCCUS AUREUS) WAS MISIDENTIFIED AS GROUP B STREP (GBS) OR STREPTOCOCCUS AGALACTIAE. THE USER VERIFIED THE FINAL RESULT USING CATALASE AND COAGULASE. THE USER ALSO NOTED PERFORMING REPEAT TESTING AND THAT THE ISOLATE WAS COAGULASE POSITIVE AND BETA HEMOLYTIC. NO HEALTH IMPACT OR CONSEQUENCE REPORTED. THIS IS REPORT 2 OF 2.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24052566 ↗MalfunctionJan 12, 2026Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED WHILE USING THE BD PHOENIX¿ PMIC/ID-107 A PATIENT ISOLATE (STAPHYLOCOCCUS AUREUS) WAS MISIDENTIFIED AS GROUP B STREP (GBS) OR STREPTOCOCCUS AGALACTIAE. THE USER VERIFIED THE FINAL RESULT USING CATALASE AND COAGULASE. THE USER ALSO NOTED PERFORMING REPEAT TESTING AND THAT THE ISOLATE WAS COAGULASE POSITIVE AND BETA HEMOLYTIC. NO HEALTH IMPACT OR CONSEQUENCE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24043548 ↗MalfunctionJan 12, 2026Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED WHILE USING THE BD PHOENIX¿ PMIC/ID-107 A PATIENT ISOLATE (STAPHYLOCOCCUS AUREUS) WAS MISIDENTIFIED AS GROUP B STREP (GBS) OR STREPTOCOCCUS AGALACTIAE. THE USER VERIFIED THE FINAL RESULT USING CATALASE AND COAGULASE. THE USER ALSO NOTED PERFORMING REPEAT TESTING AND THAT THE ISOLATE WAS COAGULASE POSITIVE AND BETA HEMOLYTIC. NO HEALTH IMPACT OR CONSEQUENCE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24043541 ↗MalfunctionDec 18, 2025Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED WHILE USING THE BD PHOENIX¿ PMIC/ID-107 A PATIENT ISOLATE (STAPHYLOCOCCUS EPIDERMIDIS) WAS MISIDENTIFIED AS STAPHYLOCOCCUS COHNII. THE USER VERIFIED THE FINAL RESULT USINGVITEK® 2 AND REPEAT TESTING. NO HEALTH IMPACT OR CONSEQUENCE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23840517 ↗MalfunctionDec 4, 2025Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED WHILE USING THE BD PHOENIX¿ PMIC/ID-107 A PATIENT URINE ISOLATE (STAPHYLOCOCCUS SAPROPHYTICUS) WAS MISIDENTIFIED AS STAPHYLOCOCCUS AUREUS. THE USER VERIFIED THE FINAL RESULT USING COAGULASE, REPEAT TESTING AND VITEK®. NO HEALTH IMPACT OR CONSEQUENCE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23719015 ↗MalfunctionDec 4, 2025Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED WHILE USING THE BD PHOENIX¿ PMIC/ID-107 A PATIENT URINE ISOLATE (STAPHYLOCOCCUS SAPROPHYTICUS) WAS MISIDENTIFIED AS STAPHYLOCOCCUS AUREUS. THE USER VERIFIED THE FINAL RESULT USING MICROBIOLOGY BACTERIAL CULTURE AND BASIC WORKUP AND A REFERENCE LABORATORY. NO HEALTH IMPACT OR CONSEQUENCE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23718946 ↗MalfunctionSep 9, 2025Incorrect Measurement; Incorrect Measurement
IT WAS REPORTED WHILE USING THE BD PHOENIX¿ PMIC/ID-(B)(6) A PATIENT URINE ISOLATE (STAPHYLOCOCCUS AUREUS) WAS MISIDENTIFIED AS STAPHYLOCOCCUS EPIDERMIDIS. THE USER ALSO NOTED QC AND SURVEILLANCE FAILURES AS WELL. NO HEALTH IMPACT OR CONSEQUENCE REPORTED. REPORT 4 OF 4.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23006386 ↗MalfunctionSep 9, 2025Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED WHILE USING THE BD PHOENIX¿ PMIC/ID-107 A PATIENT WOUND ISOLATE (STAPHYLOCOCCUS AUREUS) WAS MISIDENTIFIED AS CORYNEBACTERIUM XEROSIS. THE USER ALSO NOTED QC AND SURVEILLANCE FAILURES AS WELL. NO HEALTH IMPACT OR CONSEQUENCE REPORTED. REPORT 1 OF 4.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23006372 ↗MalfunctionSep 9, 2025Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED WHILE USING THE BD PHOENIX¿ PMIC/ID-107 A PATIENT URINE ISOLATE (STAPHYLOCOCCUS AUREUS) WAS MISIDENTIFIED AS STAPHYLOCOCCUS EPIDERMIDIS. THE USER ALSO NOTED QC AND SURVEILLANCE FAILURES AS WELL. NO HEALTH IMPACT OR CONSEQUENCE REPORTED. REPORT 3 OF 4.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23006370 ↗MalfunctionSep 9, 2025Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED WHILE USING THE BD PHOENIX¿ PMIC/ID-(B)(4) A PATIENT ISOLATE (STAPHYLOCOCCUS AUREUS) WAS MISIDENTIFIED AS STAPHYLOCOCCUS EPIDERMIDIS. THE USER ALSO NOTED QC AND SURVEILLANCE FAILURES AS WELL. NO HEALTH IMPACT OR CONSEQUENCE REPORTED. REPORT 2 OF 4.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23006365 ↗MalfunctionSep 4, 2025Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED WHILE USING BD PHOENIX¿ PMIC/ID-107, A PATIENT SAMPLE WAS INCORRECTLY IDENTIFIED. THERE WAS NO REPORT OF PATIENT IMPACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22963672 ↗MalfunctionSep 4, 2025Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED WHILE USING BD PHOENIX¿ PMIC/ID-(B)(6), A PATIENT SAMPLE WAS INCORRECTLY IDENTIFIED. THERE WAS NO REPORT OF PATIENT IMPACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22963624 ↗MalfunctionSep 4, 2025Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED WHILE USING BD PHOENIX¿ PMIC/ID-107, A PATIENT SAMPLE WAS INCORRECTLY IDENTIFIED. THERE WAS NO REPORT OF PATIENT IMPACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22963621 ↗MalfunctionSep 4, 2025Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED WHILE USING BD PHOENIX¿ PMIC/ID-107, A PATIENT SAMPLE WAS INCORRECTLY IDENTIFIED. THERE WAS NO REPORT OF PATIENT IMPACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22960963 ↗MalfunctionSep 4, 2025Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED WHILE USING BD PHOENIX¿ PMIC/ID-107, A PATIENT SAMPLE WAS INCORRECTLY IDENTIFIED. THERE WAS NO REPORT OF PATIENT IMPACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22960962 ↗MalfunctionSep 4, 2025Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED WHILE USING BD PHOENIX¿ PMIC/ID-107, A PATIENT SAMPLE WAS INCORRECTLY IDENTIFIED. THERE WAS NO REPORT OF PATIENT IMPACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22960961 ↗MalfunctionSep 4, 2025Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED WHILE USING BD PHOENIX¿ PMIC/ID-107, A PATIENT SAMPLE WAS INCORRECTLY IDENTIFIED. THERE WAS NO REPORT OF PATIENT IMPACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22960960 ↗MalfunctionSep 4, 2025Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED WHILE USING BD PHOENIX¿ PMIC/ID-107, A PATIENT SAMPLE WAS INCORRECTLY IDENTIFIED. THERE WAS NO REPORT OF PATIENT IMPACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22960959 ↗MalfunctionSep 4, 2025Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED WHILE USING BD PHOENIX¿ PMIC/ID-107, A PATIENT SAMPLE WAS INCORRECTLY IDENTIFIED. THERE WAS NO REPORT OF PATIENT IMPACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22960957 ↗MalfunctionSep 3, 2025Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED WHILE USING BD PHOENIX¿ PMIC/ID-107, A PATIENT SAMPLE WAS INCORRECTLY IDENTIFIED. THERE WAS NO REPORT OF PATIENT IMPACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22952959 ↗
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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 · each recall links to the FDA recall notice
- 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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