NMIC/ID-313 449083Recalls & reported problems
Becton, Dickinson And Company · NMIC/ID-313 · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 24
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 24 adverse event reports that list this exact device (DI 30382904490837), received between Aug 27, 2026 and Sep 30, 2026 — classified as 24 malfunctions.
The most frequently reported specific device problem is “Incorrect, Inadequate or Imprecise Result or Readings” (24 reports).
2 other recalls cover devices cleared under the same FDA submission (K020322, K023444, K023634, K023858, K033458, K042932, K060444, K060447, K061327, K061355, K062944, K062945, K063573, K063811, K063824, K132674, K181665, K233986); they may or may not involve this specific model.
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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Incorrect, Inadequate or Imprecise Result or Readings24
Patient problems
- No Clinical Signs, Symptoms or Conditions24
Recent adverse event reports
The 24 most recent of 24 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Incorrect, Inadequate or Imprecise Result or Readings
It was reported while using the Panel Phoenix NMIC/ID-313 an unspecified number of patient isolates were misidentified. No health impact or consequence reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50945873 ↗MalfunctionSep 30, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50945868 ↗MalfunctionSep 15, 2026Incorrect, Inadequate or Imprecise Result or Readings
It was reported while using the Panel Phoenix NMIC/ID-313 a patient urine isolate (Escherichia coli) was misidentified as Enterobacter cloacae. The user verified the final result using MALDI. No health impact or consequence reported.This is report 10 of 10.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50776523 ↗MalfunctionSep 15, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50776522 ↗MalfunctionSep 15, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50776521 ↗MalfunctionSep 15, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50776508 ↗MalfunctionSep 15, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50776506 ↗MalfunctionSep 15, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50776501 ↗MalfunctionSep 15, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50776497 ↗MalfunctionSep 15, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50776496 ↗MalfunctionSep 15, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50776494 ↗MalfunctionSep 15, 2026Incorrect, Inadequate or Imprecise Result or Readings
It was reported while using the Panel Phoenix NMIC/ID-313 a patient urine isolate (Escherichia coli) was misidentified as Citrobacter freundii. The user verified the final result using MALDI. No health impact or consequence reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50773754 ↗MalfunctionSep 15, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50773753 ↗MalfunctionAug 28, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50499347 ↗MalfunctionAug 28, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50499346 ↗MalfunctionAug 28, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50499343 ↗MalfunctionAug 28, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50499342 ↗MalfunctionAug 28, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50499341 ↗MalfunctionAug 28, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50499339 ↗MalfunctionAug 28, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50499338 ↗MalfunctionAug 28, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50499336 ↗MalfunctionAug 28, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50499334 ↗MalfunctionAug 27, 2026Incorrect, Inadequate or Imprecise Result or Readings
It was reported while using the BD Phoenix¿ NMIC/ID-313 a patient urine isolate (Escherichia coli) is misidentified as Enterobacter cloacae. The user stated that Maldi was used when the identification did not match the biochemical results. In addition, the user stated any non-lactose fermenting organism, or mucoid Escherichia coli is called Enterobacter cloacae. No health impact or consequence reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50482700 ↗MalfunctionAug 27, 2026Incorrect, Inadequate or Imprecise Result or Readings
It was reported while using the BD Phoenix¿ NMIC/ID-313 a patient urine isolate (Escherichia coli) is misidentified as Citrobacter freundii. The user stated that Maldi was used when the identification did not match the biochemical results. No health impact or consequence reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50482315 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K020322, K023444, K023634, K023858, K033458, K042932, K060444, K060447, K061327, K061355, K062944, K062945, K063573, K063811, K063824, K132674, K181665, K233986. One submission often covers many models, so check the product and lot details in each record.
- Z-1398-2024 · Feb 29, 2024 · Open, ClassifiedBD Phoenix NMIC-306 Panel is a self-inoculating (when used with a BD Phoenix Automated Microbiology System) polystyrene panel (tray) containing control wells and substrate wells wi
- Z-1847-2011 · Feb 28, 2011 · TerminatedBD Phoenix" Panel NMIC/ID-123, Catalog # 448723, packaged 25 panels/carton, and labeled in part ***Becton, Dickinson and Company 7 Loveton Circle Sparks, MD 21152 USA (800) 638-866
Other SYSTEM, TEST, AUTOMATED, ANTIMICROBIAL SUSCEPTIBILITY, SHORT INCUBATION devices
- BD Phoenix™ M50 Automated Microbiology System 443624Becton, Dickinson And Company · SYSTEM, TEST, AUTOMATED, ANTIMICROBIAL SUSCEPTIBILITY, SHORT INCUBATION3 recalls417 reports
- BD Phoenix™ NMIC/ID-307 449289Becton, Dickinson And Company · SYSTEM, TEST, AUTOMATED, ANTIMICROBIAL SUSCEPTIBILITY, SHORT INCUBATION529 reports
- BD Phoenix™ PMIC/ID-107 448607Becton, Dickinson And Company · SYSTEM, TEST, AUTOMATED, ANTIMICROBIAL SUSCEPTIBILITY, SHORT INCUBATION2 recalls169 reports
- BD Phoenix™ NMIC-306 449292Becton, Dickinson And Company · SYSTEM, TEST, AUTOMATED, ANTIMICROBIAL SUSCEPTIBILITY, SHORT INCUBATION1 recall143 reports
- VITEK® 2 AST-GP67Biomerieux , Inc. · System, Test, Automated, Antimicrobial Susceptibility, Short Incubation2 recalls83 reports
- BD Phoenix™ AST Broth 246003Becton, Dickinson And Company · SYSTEM, TEST, AUTOMATED, ANTIMICROBIAL SUSCEPTIBILITY, SHORT INCUBATION182 reports
- VITEK® 2 AST-GP75Biomerieux , Inc. · System, Test, Automated, Antimicrobial Susceptibility, Short Incubation2 recalls52 reports
- VITEK® 2 AST-GP78Biomerieux , Inc. · System, Test, Automated, Antimicrobial Susceptibility, Short Incubation2 recalls41 reports
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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