Pyxis Pro MedStation 177-184Recalls & 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
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10885403521294), received between Oct 9, 2025 and Oct 10, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Activation Failure” (1 report).
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
- Activation Failure1
- Loose or Intermittent Connection1
- No Apparent Adverse Event1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 10, 2025Loose or Intermittent Connection; Activation Failure; Loose or Intermittent Connection; Activation Failure
IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ PRO REFRIGERATOR, THAT MULTIPLE DRAWERS WERE FAILED. THE CUSTOMER STATED THAT THERE WAS A DELAY IN DISPENSING MEDICATION TO A PATIENT. THERE WERE NO ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23264816 ↗MalfunctionOct 9, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ PRO REFRIGERATOR, TOWER AUXILIARY AND BIN WAS FAILED TO RECOVER. THE CUSTOMER STATED THERE WAS A DELAY TO THE PATIENT'S WORKFLOW. THERE WERE NO ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23253521 ↗
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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