BD Phoenix™ NMIC/ID-304 448743Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 30382904487431), received between Jun 16, 2020 and Aug 18, 2023 — classified as 1 injury, 2 malfunctions.

The most frequently reported specific device problem is “Complete Blockage” (2 reports).

2 other recalls cover devices cleared under the same FDA submission (K020322, K023444, K023634, K023858, K023895, K024153, K031530, K031699, K031912, K032299, K032655, K032675, K033458, K033558, K033560, K041384, K042932, K052269, K060214, K060217, K060444, K060447, K061327, K061355, K061867, K062944, K063301, K063573, K063811, K063824, K123266, K123404, K132674); 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 18, 2026.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 18, 2023Complete Blockage; Complete Blockage

  IT WAS REPORTED THAT THE BD MICROLANCE ¿ 3 NEEDLE WAS BLOCKED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM FRENCH TO ENGLISH: BLOCKED NEEDLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17572885 ↗
• MalfunctionAug 11, 2023Complete Blockage; Complete Blockage

  IT WAS REPORTED THAT WHILE USING THE BD MICROLANCE ¿ 3 NEEDLES IT GETS CLOGGED.THE FOLLOWING WAS RECEIVED FROM THE INITIAL REPORTER: WE SOMETIMES USE 3 OR 4 TROCARS TO INJECT INTO THE IV BECAUSE IT GETS CLOGGED++.

  Patient problems: Insufficient Information

  MAUDE report 17515348 ↗
• InjuryJun 16, 2020Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings

  IT WAS REPORTED THAT WHILE USING THE PANEL PHOENIX NMIC ID 304, AN ERRONEOUS RESULTS WAS REPORTED. THE PANEL USED, MISIDENTIFIED KLEBSIELLA AEROGENES AS ENTEROBACTER CLOACAE. PATIENT RESULTS WERE REPORTED AND THE PATIENT RECEIVED TREATMENT. CONFIRMATORY TESTING WAS PERFORMED AND A CORRECTED REPORT WAS SENT TO THE PHYSICIAN.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10159615 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K020322, K023444, K023634, K023858, K023895, K024153, K031530, K031699, K031912, K032299, K032655, K032675, K033458, K033558, K033560, K041384, K042932, K052269, K060214, K060217, K060444, K060447, K061327, K061355, K061867, K062944, K063301, K063573, K063811, K063824, K123266, K123404, K132674. One submission often covers many models, so check the product and lot details in each record.

• Z-1398-2024 · Feb 29, 2024 · Open, Classified
  BD 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 · Terminated
  BD 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