BD Pyxis 309Recalls & reported problems
Carefusion 303, Inc. · BD Pyxis MedStation 4000 Integrated Main · Class 1
All models of BD Pyxis (26)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
Quick summary
This BD Pyxis medication cabinet is a console used to dispense medications. Reports describe software and console glitches—login failures, black screens, stuck drawers, and delayed medication dispensing—without injuries. There are 80 reports: 80 malfunctions, no deaths, no injuries. No recalls name this device. Reports fell to 26 in the last 12 months from 53 the prior 12 months.
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
- 82
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 82 adverse event reports that list this exact device (DI 10885403512643), received between Jun 11, 2024 and Sep 28, 2026 — classified as 82 malfunctions.
The most frequently reported specific device problem is “Computer Software Problem” (35 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Computer Software Problem35
- Application Program Problem14
- Communication or Transmission Problem13
- Labelling, Instructions for Use or Training Problem5
- Activation Failure4
- Application Program Freezes or Fails to Launch4
- Application Network Problem3
- Mechanical Problem3
Patient problems
- No Clinical Signs, Symptoms or Conditions82
Recent adverse event reports
The 25 most recent of 82 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 28, 2026Application Program Problem
It was reported that when using the BD Pyxis¿ MedStation¿ 4000 CONSOLE duplicate patient admissions were displayed for the second time. The customer reported that MRN (b)(4), who was currently admitted to the Maternity unit, was also appearing in the Pyxis system as an active admission in the medical unit from 2025. As a result of the duplicate admission record, nursing staff were unable to access or remove certain medications for the patient, causing workflow disruption.The customer stated 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 50913268 ↗MalfunctionSep 14, 2026No Apparent Adverse Event
It was reported by the customer that when using the BD Pyxis¿ MedStation¿ 4000 CONSOLE, a patient who remained active in the Cerner was unexpectedly discharged from the Pyxis system. The customer reported that a malfunction took place when the user tried to dispense medication to the patient. 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 50755337 ↗MalfunctionAug 20, 2026Application Program Problem
It was reported that when using the BD Pyxis¿ MedStation¿ 4000 CONSOLE, medication order frequencies were sent to Pyxis through an interface message and were mapped in the External Order Frequency Codes section of Pyxis ES, allowing nurses to view medication due times aligned with the MAR in Epic. The customer stated that there was a delay in patient care. There were no adverse events or injuries reported based on this incident.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50342835 ↗MalfunctionAug 13, 2026Labelling, Instructions for Use or Training Problem
It was reported that when using the BD Pyxis¿ MedStation¿ 4000 CONSOLE all users were unable to login. The machine suddenly logged out, and no one know the credentials required to log back 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 50233321 ↗MalfunctionJun 18, 2026Loose or Intermittent Connection
IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ MEDSTATION¿ 4000 CONSOLE, THE DRAWER FAILED AND THE RECOVERY SCREEN WAS FILLED WITH MULTIPLE DRAWERS THAT WERE UNABLE TO BE RECOVERED. 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 25549983 ↗MalfunctionJun 17, 2026Battery Problem
IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ MEDSTATION¿ 4000 CONSOLE BATTERY STARTED FLASHING, PRODUCED A BEEPING SOUND AND WENT OFFLINE ON REMOTE SUPPORT SERVICE. THE CUSTOMER STATED THAT THIS MALFUNCTION OCCURRED WHILE DISPENSING THE MEDICATION AND THE USER MANAGED TO GET THE MEDICATION FROM OTHER SOURCES, WHICH CAUSED A DELAY TO THE PATIENT CARE. THERE WERE NO ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25532511 ↗MalfunctionMay 13, 2026Application Program Problem; Application Program Freezes or Fails to Launch
IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ MEDSTATION¿ 4000 CONSOLE, THE MEDICATION APPLICATION WAS UNABLE TO LAUNCH AND TOOK MORE SPACE IN C DRIVE. THE CUSTOMER STATED THAT THIS MALFUNCTION CAUSED A DELAY IN DISPENSING MEDICATION TO PATIENTS. THERE WERE NO ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25160216 ↗MalfunctionMay 12, 2026Application Program Problem
IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ MEDSTATION¿ 4000 CONSOLE THE SCREEN WAS NOT FUNCTIONING AND REMAINED STUCK ON A BLACK SCREEN, AND THE CUSTOMER REBOOTED THE STATION, BUT THE ISSUE PERSISTED. 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 25148835 ↗MalfunctionApr 25, 2026Labelling, Instructions for Use or Training Problem
IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ MEDSTATION¿ 4000 CONSOLE, USER UNABLE TO USE PYXIS DEVICES. THE CUSTOMER STATED THAT THIS MALFUNCTION OCCURRED WHILE DISPENSING THE MEDICATION AND CAUSED A DELAY TO THE PATIENT CARE. THERE WERE NO ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24991637 ↗MalfunctionApr 23, 2026Contamination; Activation Failure
IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ MEDSTATION¿ 4000 CONSOLE, THE DRAWER WAS BROKEN AND WAS IN FAILURE MODE. 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 24963089 ↗MalfunctionApr 14, 2026Mechanical Problem
IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ MEDSTATION¿ 4000 CONSOLE, THE DRAWERS HAD FAILED AND COULD NOT BE RECOVERED. THE CUSTOMER STATED 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 24873076 ↗MalfunctionMar 23, 2026Labelling, Instructions for Use or Training Problem
IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ MEDSTATION¿ 4000 INTEGRATED MAIN, THE USER WAS UNABLE TO LOG IN USER ID AND PASSWORD, BUT THE ERROR SHOWN ON NON LIVE AT SERVER. THE CUSTOMER REPORTED THAT THE ISSUE OCCURRED WHEN THE USER WAS TRYING TO ISSUE MEDICATIONS TO A PATIENT. THERE WERE NO DELAY, NO ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24662650 ↗MalfunctionMar 19, 2026Application Program Problem
IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ MEDSTATION¿ 4000 CONSOLE, THREE DRAWERS ON THREE SEPARATE FLOORS WERE NOT DETECTED ON THE BUS. ONE DRAWER HAD FAILED BEFORE THE POWER SURGE, AND TWO ADDITIONAL DRAWERS POSSIBLY FAILED AFTERWARD. THE CUSTOMER STATED 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 24637492 ↗MalfunctionMar 18, 2026Application Network Problem
IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ MEDSTATION¿ 4000 CONSOLE, THERE WAS NO COMMUNICATION WITH THE WORKSTATIONS, AND THE UNIT APPEARED OFFLINE IN REMOTE SMART SERVICES (RSS). 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 24625874 ↗MalfunctionMar 3, 2026Application Network Problem; Installation-Related Problem
IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ MEDSTATION¿ 4000 CONSOLE DEVICE WAS NOT LISTED AND THE UNIT WAS NOT COMMUNICATING WITH THE MAIN UNIT. 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 24494628 ↗MalfunctionJan 22, 2026Activation Failure
IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ MEDSTATION¿ 4000 CONSOLE CUBIE DRAWER FAILED TO OPEN AND USER HAD EXPERIENCED A LOUD CLICKING SOUND, UNABLE TO RECOVER IT. THE CUSTOMER STATED 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 24143249 ↗MalfunctionJan 22, 2026Application Program Problem; Activation Failure
IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ ES REFRIGERATOR 3NEE COMPARTMENT WAS NOT ACCESSIBLE. THE INDICATOR LIGHT ON THE SMALL BOX WAS NOT ILLUMINATED, AND THE COMPARTMENT DID NOT ATTEMPT TO OPEN ELECTRONICALLY. THE CUSTOMER CONFIRMED IT COULD BE OPENED MANUALLY USING A KEY, HOWEVER DURING ATTEMPTED RECOVERY OF THE FAILED STORAGE, THE COMPARTMENT DID NOT ATTEMPT TO OPEN AT ALL. 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 24143077 ↗MalfunctionDec 16, 2025Application Program Problem; Application Program Problem
IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ MEDSTATION¿ 4000 CONSOLE, HAD WRONG TIME DIFFERENCE WITH MAIN PHARMACY WHILE PULLING MEDICATIONS. THE CUSTOMER STATED 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 23815020 ↗MalfunctionDec 5, 2025Circuit Failure; Circuit Failure
IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ MEDSTATION¿ 4000 CONSOLE DEVICE NOT DETECTED ON BUS. THE CUSTOMER STATED 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 23727816 ↗MalfunctionNov 15, 2025Application Program Problem; Application Program Problem
IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ MEDSTATION¿ 4000 CONSOLE THE SCREEN WAS WHITE BLANK AND NO SINGLE MEDICATION LIST OUT. 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 23563649 ↗MalfunctionNov 7, 2025Application Program Problem; Application Program Problem
IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ MEDSTATION¿ 4000 CONSOLE, THE SERVER HAD INTERNAL ERROR MESSAGE. THE CUSTOMER STATED THAT THIS MALFUNCTION CAUSED A DELAY IN DISPENSING MEDICATION TO PATIENTS. THERE WERE NO ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23496230 ↗MalfunctionNov 6, 2025Computer Software Problem; Computer Software Problem
IT WAS REPORTED BY THE CUSTOMER THAT A BD PYXIS MEDSTATION 4000 CONSOLE SYSTEM COULD NOT ACCESS THE MED STATION 4000 AND NEEDED USERNAME AND PASSWORD. WHEN THE USER TRIED TO RETRIEVE THE MEDICATION AT THE DISPENSER AND OPENED THE PATIENT THE PATIENT SPECIFIC PROFILE 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 23484237 ↗MalfunctionNov 6, 2025Computer Software Problem; Computer Software Problem
IT WAS REPORTED BY THE CUSTOMER THAT A MEDSTATION 4000 CONSOLE WAS UNABLE TO PULL MEDICATION FOR A PATIENT. THERE WERE NO ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS INCIDENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23483417 ↗MalfunctionNov 5, 2025Computer Software Problem; Computer Software Problem
IT WAS REPORTED BY THE CUSTOMER THAT A BD PYXIS MEDSTATION ES SYSTEM WAS UNABLE TO REMOVE MEDICATION DUE TO AN INVALID MULTI-COMPONENT ORDER. THERE WERE NO ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS INCIDENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23473653 ↗MalfunctionNov 4, 2025Computer Software Problem; Computer Software Problem
IT WAS REPORTED BY THE CUSTOMER THAT A BD PYXIS¿ MEDSTATION¿ 4000 CONSOLE PATIENT ORDERS FAILED TO BE CROSSED FROM THE INTERFACE AND THE CUSTOMER STATED THAT DUE TO THIS ISSUE THEY WERE UNABLE TO RECEIVED MEDICATION FOR PATIENTS. THERE WERE NO ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS INCIDENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23463277 ↗
Other CABINET, TABLE AND TRAY, ANESTHESIA devices
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- 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
- 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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