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BD Pyxis 323 (UDI 10885403533228)Recalls & reported problems

Carefusion 303, Inc. · BD Pyxis MedStation ES (Main) · Class 1

Quick summary

This BD Pyxis MedStation ES cabinet has 25,588 adverse event reports in the FDA database, including 2 deaths and 5 injuries. Recent reports mostly describe drawers that fail, software that freezes, and delays in getting medication. No recalls name this device. Reports in the last 12 months (23,080) are far higher than in the 12 months before (2,508).

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
28,053
Deaths reported
2
Injuries reported
5
Recalls naming it
0

Summary

The FDA's MAUDE database contains 28,053 adverse event reports that list this exact device (DI 10885403533228), received between Jan 2, 2025 and Sep 30, 2026 — classified as 2 deaths, 5 injuries, 28,028 malfunctions.

The most frequently reported specific device problem is “Mechanical Problem” (5,256 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

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 34 reportsFeb 2025: 108 reportsMar 2025: 119 reportsApr 2025: 132 reportsMay 2025: 136 reportsJun 2025: 123 reportsJul 2025: 99 reportsAug 2025: 170 reportsSep 2025: 464 reportsOct 2025: 1,123 reportsNov 2025: 1,939 reportsDec 2025: 2,949 reportsJan 2026: 1,602 reportsFeb 2026: 2,077 reportsMar 2026: 2,343 reportsApr 2026: 2,098 reportsMay 2026: 2,443 reportsJun 2026: 2,782 reportsJul 2026: 2,703 reportsAug 2026: 2,081 reportsSep 2026: 2,528 reportsOct 2026: 0 reports2024202520262,949
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Mechanical Problem5,256
  • Loose or Intermittent Connection4,682
  • Circuit Failure4,182
  • Application Program Problem3,634
  • Break3,080
  • Electrical /Electronic Property Problem3,073
  • Labelling, Instructions for Use or Training Problem1,611
  • No Apparent Adverse Event1,484

Patient problems

  • No Clinical Signs, Symptoms or Conditions28,040
  • Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available8
  • Insufficient Information3
  • Loss of consciousness2
  • Cardiac Arrest1
  • Chest Pain1
  • Dyspnea1
  • Hypoglycemia1

Recent adverse event reports

The 25 most recent of 28,053 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 30, 2026Break; Circuit Failure; Mechanical Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50953973 ↗
  • MalfunctionSep 30, 2026Application Program Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50953970 ↗
  • MalfunctionSep 30, 2026Loose or Intermittent Connection

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50953967 ↗
  • MalfunctionSep 30, 2026Application Network Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50953965 ↗
  • MalfunctionSep 30, 2026Circuit Failure; Loose or Intermittent Connection

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50953961 ↗
  • MalfunctionSep 30, 2026Electrical /Electronic Property Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50953960 ↗
  • MalfunctionSep 30, 2026Circuit Failure

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50953959 ↗
  • MalfunctionSep 30, 2026Electrical /Electronic Property Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50953958 ↗
  • MalfunctionSep 30, 2026Loose or Intermittent Connection

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50953957 ↗
  • MalfunctionSep 30, 2026Loose or Intermittent Connection; Mechanical Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50953955 ↗
  • MalfunctionSep 30, 2026Circuit Failure; Electrical /Electronic Property Problem; Mechanical Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50953953 ↗
  • MalfunctionSep 30, 2026Electrical /Electronic Property Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50953952 ↗
  • MalfunctionSep 30, 2026Break; Mechanical Jam

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50953947 ↗
  • MalfunctionSep 30, 2026Loose or Intermittent Connection

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50953945 ↗
  • MalfunctionSep 30, 2026Circuit Failure

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50953944 ↗
  • MalfunctionSep 30, 2026Mechanical Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50953942 ↗
  • MalfunctionSep 30, 2026Loose or Intermittent Connection

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50953937 ↗
  • MalfunctionSep 30, 2026Mechanical Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50953936 ↗
  • MalfunctionSep 30, 2026Electrical /Electronic Property Problem; Loose or Intermittent Connection

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50953935 ↗
  • MalfunctionSep 30, 2026Mechanical Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50953934 ↗
  • MalfunctionSep 30, 2026No Apparent Adverse Event

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50953933 ↗
  • MalfunctionSep 30, 2026Loose or Intermittent Connection; Mechanical Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50953932 ↗
  • MalfunctionSep 30, 2026Circuit Failure; Application Program Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50953929 ↗
  • MalfunctionSep 30, 2026Contamination; Loose or Intermittent Connection

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50953928 ↗
  • MalfunctionSep 30, 2026Circuit Failure; Loose or Intermittent Connection

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50953927 ↗

Other Cabinet, table and tray, anesthesia devices

All Cabinet, table and tray, anesthesia devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.