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BD Pyxis MEDBANK-MINI-AUXRecalls & reported problems

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

All models of BD Pyxis (26)

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.

Adverse event reports
7
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 10885403512551), received between Nov 12, 2025 and Sep 22, 2026 — classified as 7 malfunctions.

The most frequently reported specific device problem is “Application Program Problem” (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 18, 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: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 2 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 1 reportsMar 2026: 2 reportsApr 2026: 1 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 1 reportsOct 2026: 0 reports2024202520262
Last 36 months. The most recent month may be incomplete.

Recalls naming this device

  1. Sep 30, 2025Class IIOpen, 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

  • Application Program Problem2
  • Communication or Transmission Problem1
  • Computer Software Problem1
  • Electrical /Electronic Property Problem1
  • Failure to Eject1
  • Installation-Related Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions7

Recent adverse event reports

The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 22, 2026Electrical /Electronic Property Problem

    It was reported that when using the BD Pyxis¿ MedBank Mini Aux, system cubie lid was not opening. The customer reported that a malfunction took place when the user tried to dispense medication to the patient. However, there were no delay or adverse events or injuries reported based on this event.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50852206 ↗
  • MalfunctionApr 16, 2026Application Program Problem

    IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ MEDBANK MINI AUX DRAWERS WERE OFFLINE AND WAS UNABLE TO LOG IN. 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 24894180 ↗
  • MalfunctionMar 23, 2026Application Program Problem

    IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ MEDBANK MINI AUX USER WAS UNABLE TO ISSUE THE MEDICATION BECAUSE IT WAS NOT LISTED ON THE PATIENT PROFILE, AND THE USER DOES NOT HAVE THE APPROPRIATE OVERRIDE PERMISSIONS. 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 24659956 ↗
  • MalfunctionMar 13, 2026Installation-Related Problem

    IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ MEDBANK MINI AUX, DRAWER WAS NOT OPENING. THE CUSTOMER STATED THAT THEY WERE UNABLE TO ISSUE THE MEDICATION. THERE WERE NO ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS EVENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24592833 ↗
  • MalfunctionFeb 24, 2026Communication or Transmission Problem

    IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ MEDBANK MINI AUX, THE DRAWERS 12 &13 WAS FAILED TO OPEN AND NOT DETECTED ON BUS. AS PER PART INVESTIGATION, IT WAS DETERMINED THAT THERE WAS DAMAGED PCBA COMPONENTS AND DAMAGED PLASTIC COVER OF INDUCTOR L302 UNDER MICROSCOPE. THERE WERE NO DELAY, NO ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS EVENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24426582 ↗
  • MalfunctionNov 13, 2025Failure to Eject; Failure to Eject

    IT WAS REPORTED BY THE CUSTOMER THAT A BD PYXIS MEDBANK SYSTEM CUBIE DID NOT OPEN WHILE TRIED TO ISSUE THE MEDICATION FROM THE PYXIS. THERE WERE NO ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS INCIDENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23540771 ↗
  • MalfunctionNov 12, 2025Computer Software Problem; Computer Software Problem

    IT WAS REPORTED BY THE CUSTOMER THAT AT BD PYXIS¿ MEDBANK MINI NO MEDS WERE FOUND IN POCKET, BUT IT WAS SAYING COUNT WAS 15 WHILE ISSUING BUSPIRONE 15MG TAB ON (B)(6). THERE WERE NO ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS INCIDENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23533025 ↗

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Sources and updates

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