Pyxis Pro MedStationRecalls & reported problems across all models
Carefusion 303, Inc. · 6 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
3 open recalls name at least one Pyxis Pro MedStation model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 33
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 3
We found 6 models of Pyxis Pro MedStation by Carefusion 303, Inc. in the FDA's device registry (GUDID). Together they are named in 33 adverse event reports in the FDA's MAUDE database, received between Oct 9, 2025 and Sep 26, 2026 — classified as 33 malfunctions.
The most frequently reported specific device problem is “Application Program Problem” (7 reports).
3 FDA recall records name at least one of these models by its device identifier, 3 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Pyxis Pro MedStation recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Nov 20, 2025Open, Classified
Automated Dispensing Cabinets (ADC) received a Half Height CUBIE drawer firmware update, which caused a Cubie Insert event which prompts software to generate a duplicate address, which causes an error and the drawer to fail, which may lead to inability or delay in accessing stored items, delay in the replenishment of ADCs or patient specific medications stored outside of ADCs.
Z-0962-2026 · Root cause: Device Design · names 3 of these models · Recall details · FDA record ↗
- Sep 30, 2025Open, Classified
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
Z-0370-2026 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Sep 30, 2025Open, Classified
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
Z-0369-2026 · Root cause: Under Investigation by firm · names 2 of these models · Recall details · FDA record ↗
Most reported Pyxis Pro MedStation problems
Device problems
- Application Program Problem7
- Mechanical Problem7
- Electrical /Electronic Property Problem5
- No Apparent Adverse Event4
- Activation Failure3
- Break3
- Failure to Align3
- Labelling, Instructions for Use or Training Problem3
Patient problems
- No Clinical Signs, Symptoms or Conditions33
Pyxis Pro MedStation models
6 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Pyxis Pro MedStation 1155-00Cabinet, table and tray, anesthesia2 recalls23 reports
- Pyxis Pro MedStation 1149-00Cabinet, table and tray, anesthesia2 recalls4 reports
- Pyxis Pro MedStation 1152-00Cabinet, table and tray, anesthesia2 recalls2 reports
- Pyxis Pro MedStation 177-184Cabinet, table and tray, anesthesia2 reports
- Pyxis Pro MedStation 177-138Cabinet, table and tray, anesthesia1 report
- Pyxis Pro MedStation 177-255Cabinet, table and tray, anesthesia1 report
Recent Pyxis Pro MedStation adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 26, 2026Mechanical Jam
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50908098 ↗MalfunctionSep 22, 2026Failure to Align
It was reported that when using the BD Pyxis¿ Pro MedStation¿ Main, refrigerator in the pyxis frequently displayed a "refrigerator fail" error. The issue occurred repeatedly and was suspected to be related to lock or door alignment problems. The customer stated that the malfunction occurred when a user tried to issue medication to the patient and caused a delay to patient care. However, there were no adverse events or injuries reported based on this event.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50850746 ↗MalfunctionSep 21, 2026Contamination
It was reported that when using the BD Pyxis¿ Pro MedStation¿ ES Biometric Identifier failed and was unable to scan. The customer attempted to reboot the station multiple times; however, the issue persisted.The customer stated that this malfunction occurred while dispensing the medication 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 50839394 ↗MalfunctionSep 18, 2026Break; Electrical /Electronic Property Problem; Mechanical Problem
It was reported that when using the BD Pyxis¿ Pro MedStation Aux, the drawer 2 and 3 had experienced a recurring failure issue. The customer stated that this malfunction occurred while dispensing the medication 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 50814726 ↗MalfunctionSep 16, 2026No Apparent Adverse Event
It was reported that when using the BD Pyxis¿ Pro Refrigerator unable to access the bin. Customer stated that while recovering storage space, it would open but remain stuck on the message, "Please pull open", even after they had pulled it open and closed it.The customer stated that this malfunction occurred while dispensing the medication 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 50792517 ↗MalfunctionSep 9, 2026Application Program Problem
It was reported that when using the BD Pyxis¿ Pro MedStation Aux, the drawer was broken. The customer stated that the malfunction occurred when a user tried to issue medication to the patient and caused a delay to patient care. However, there were no adverse events or injuries reported based on this event.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50688726 ↗MalfunctionSep 7, 2026No Apparent Adverse Event; Activation Failure
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50648901 ↗MalfunctionSep 7, 2026Labelling, Instructions for Use or Training Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50646221 ↗MalfunctionAug 31, 2026Labelling, Instructions for Use or Training Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50523149 ↗MalfunctionAug 28, 2026Use of Device Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50494177 ↗MalfunctionAug 27, 2026Application Program Problem
It was reported that when using the BD Pyxis¿ Pro MedStation¿ ES, user synchronized a username with another user badge.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 50469709 ↗MalfunctionAug 26, 2026Application Program Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50454332 ↗MalfunctionAug 20, 2026Application Program Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50358824 ↗MalfunctionAug 12, 2026Electrical /Electronic Property Problem
It was reported that when using the BD Pyxis¿ Pro MedStation Main station displayed a black, blank screen and was completely unresponsive. The customer stated that the station remained on a black screen with no visible content. A reboot of the station was attempted; however, the issue persisted and the station did not recover.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 50219023 ↗MalfunctionJul 29, 2026Break; Loose or Intermittent Connection; Mechanical Problem; Activation Failure
It was reported that when using the BD Pyxis¿ Pro MedStation Secure Tower Aux, tower 1 had latch issue and it was intermittently failing.The customer stated that this malfunction occurred while dispensing the medication 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 50070569 ↗
Other Carefusion 303, Inc. products
- BD Alaris Infusion System29 models · 1,242,913 reports · 16 recalls
- Alaris25 models · 1,236,345 reports · 16 recalls
- BD Pyxis26 models · 81,193 reports · 66 recalls
- Pyxis5 models · 7,862 reports · 16 recalls
- BD Alaris PCU Model 80153 models · 4,071 reports · 2 recalls
- BD Alaris Syringe Module, Model 81102 models · 3,183 reports · 2 recalls
- BD Alaris PCU Module, Model 80152 models · 3,078 reports · 3 recalls
- Alaris PCA Module, Model 81202 models · 918 reports · 2 recalls
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- 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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