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BD Pyxis 1146-00Recalls & reported problems

Carefusion 303, Inc. · BD Pyxis MedBank Tower Auxiliary · Class 1

All models of BD Pyxis (26)

Data updated Oct 16, 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.

Adverse event reports
10
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

The FDA's MAUDE database contains 10 adverse event reports that list this exact device (DI 10885403517174), received between Jan 31, 2025 and Sep 22, 2026 — classified as 10 malfunctions.

The most frequently reported specific device problem is “Failure to Eject” (2 reports).

1 FDA recall record 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 16, 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: 1 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 1 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 1 reportsNov 2025: 3 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 1 reportsApr 2026: 1 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 1 reportsAug 2026: 0 reportsSep 2026: 1 reportsOct 2026: 0 reports2024202520263
Last 36 months. The most recent month may be incomplete.

Recalls naming this device

  1. Sep 30, 2025Open, Classified

    Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.

    Z-0367-2026 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

Most reported problems

Device problems

  • Failure to Eject2
  • Application Program Freezes or Fails to Launch1
  • Application Program Problem1
  • Break1
  • Circuit Failure1
  • Communication or Transmission Problem1
  • Electrical /Electronic Property Problem1
  • Inadequate or Insufficient Training1

Patient problems

  • No Clinical Signs, Symptoms or Conditions10

Recent adverse event reports

The 10 most recent of 10 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 22, 2026Break

    It was reported that when using the BD Pyxis¿ MedBank Tower Aux matrix drawer 16 row board issue was encountered. The customer reported having a cubie removed from the drawer and was unsure of its correct storage location.However, there were no delays or adverse events or injuries reported based on this event.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50853247 ↗
  • MalfunctionJul 28, 2026Electrical /Electronic Property Problem

    It was reported that when using the BD Pyxis¿ MedBank Tower Aux drawer opened, but the cubie did not open.The customer stated that this malfunction occurred while dispensing the medication.There were no adverse events or injuries reported based on this event.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50052004 ↗
  • MalfunctionApr 7, 2026Communication or Transmission Problem

    IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ MEDBANK TOWER AUX, THE USER WAS UNABLE TO LOG IN TO ISSUE ITEMS AND CUBEX APP WAS NOT RESPONDING. THE CUSTOMER STATED THAT THIS MALFUNCTION OCCURRED WHILE DISPENSING THE MEDICATION. HOWEVER, THERE WERE NO DELAYS OR ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS EVENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24797362 ↗
  • MalfunctionMar 24, 2026Circuit Failure

    IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ MEDBANK TOWER AUX, THE DRAWER DID NOT OPEN DURING A MEDICATION ISSUE. DRAWER 15 AND DRAWER 16 WERE DISPLAYED IN YELLOW ON THE POPULATE BUTTONS MENU. THE CUSTOMER REPORTED THAT THERE WAS A DELAY IN PATIENT CARE. THERE WERE NO ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS EVENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24673518 ↗
  • MalfunctionNov 11, 2025Inadequate or Insufficient Training; Inadequate or Insufficient Training

    IT WAS REPORTED BY THE CUSTOMER THAT A BD PYXIS MEDBANK SYSTEM WAS UNABLE TO REMOVE TO MEDICATION FENTANYL. THERE WERE NO ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS INCIDENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23520083 ↗
  • MalfunctionNov 11, 2025Failure to Eject; Failure to Eject

    IT WAS REPORTED BY THE CUSTOMER THAT A BD PYXIS¿ MEDBANK TOWER AUX SYSTEM HAD DRAWERS THAT DID NOT OPEN. THERE WERE NO ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS INCIDENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23519831 ↗
  • MalfunctionNov 7, 2025Failure to Eject; Failure to Eject

    IT WAS REPORTED BY THE CUSTOMER THAT AT BD PYXIS¿ MEDBANK TOWER AUX DRAWERS WERE NOT ONLINE. WHILE TRYING TO ISSUE MEDICATION 2 DIFFERENT OXYCODONE TAB 5MG SHOWED UP AND ONE OF THEM WAS AN EXTERNAL ITEM SWITCH SHOULD NOT BE THERE. AS WELL AS WHILE TRYING TO ISSUE THE MEDICATION NO DRAWERS WERE OPENED UP, AFTER REMOTING IN WAS FOUND THAT THE DRAWERS WERE OFFLINE AND NOT ABLE TO BE ACCESSED. THERE WERE NO ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS INCIDENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23495833 ↗
  • MalfunctionOct 16, 2025Application Program Problem; Application Program Problem

    IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ MEDBANK TOWER AUX DRAWER WAS NOT OPEN WHEN USER TRIED TO ISSUE MEDICATION. THE CUSTOMER REPORTED THAT A MALFUNCTION OCCURRED WHILE THE USER WAS ATTEMPTING TO DISPENSE MEDICATION TO THE PATIENT. THERE WERE NO ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS EVENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23309549 ↗
  • MalfunctionJun 23, 2025Application Program Freezes or Fails to Launch; Application Program Freezes or Fails to Launch

    IT WAS REPORTED BY THE CUSTOMER THAT A BD PYXIS¿ MEDBANK TOWER'S CUBEX APP WAS FROZEN WHILE ISSUING FENTANYL. THERE WERE NO ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS INCIDENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 22311307 ↗
  • MalfunctionJan 31, 2025Mechanical Problem; Mechanical Problem

    IT WAS REPORTED THAT THE PYXIS MEDBANK ES SYSTEM DRAWERS FAILED TO OPEN WHEN USERS TRIED TO ACCESS MEDICATION. THE CUSTOMER STATED THAT THERE WAS A DELAY IN DISPENSING MEDICATION. THERE WERE NO ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS EVENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21280661 ↗

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Sources and updates

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