Pyxis Pro MedStation 177-138Recalls & reported problems
Carefusion 303, Inc. · Pyxis Pro MedStation Dispensing System cabinet, table and tray, anesthesia · Class 1
All models of Pyxis Pro MedStation (6)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10885403521270), received between Sep 16, 2026 and Sep 16, 2026 — classified as 1 malfunction.
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
Most reported problems
Device problems
- No Apparent Adverse Event1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
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 ↗
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
- 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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