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
Recalls naming this device
- 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 ↗
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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