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
Recalls naming this device
- 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 ↗
Other CABINET, TABLE AND TRAY, ANESTHESIA devices
- BD Pyxis 323Carefusion 303, Inc. · Cabinet, table and tray, anesthesia2 deaths28,053 reports
- BD Pyxis 323Carefusion 303, Inc. · CABINET, TABLE AND TRAY, ANESTHESIA14 recalls2 deaths24,375 reports
- BD Pyxis 324Carefusion 303, Inc. · Cabinet, table and tray, anesthesia8,624 reports
- BD Pyxis 324Carefusion 303, Inc. · CABINET, TABLE AND TRAY, ANESTHESIA5 recalls1 death5,301 reports
- BD Pyxis 343Carefusion 303, Inc. · CABINET, TABLE AND TRAY, ANESTHESIA2 recalls1 death5,196 reports
- Pyxis 327Carefusion 303, Inc. · Cabinet, table and tray, anesthesia1 death4,304 reports
- BD Pyxis MEDBANK-TOWERCarefusion 303, Inc. · CABINET, TABLE AND TRAY, ANESTHESIA30 recalls2,581 reports
- Pyxis 327Carefusion 303, Inc. · CABINET, TABLE AND TRAY, ANESTHESIA10 recalls3,137 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 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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