BD Pyxis 1148-00Recalls & reported problems
Carefusion 303, Inc. · BD Pyxis MedBank Mini 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
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10885403517198), received between Jun 30, 2025 and May 11, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Communication or Transmission Problem” (1 report).
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
- Communication or Transmission Problem1
- Failure to Eject1
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.
MalfunctionMay 11, 2026Communication or Transmission Problem
IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ MEDBANK MINI AUX, CABINET WAS OFFLINE AND NOT SYNCHRONIZING WITH MYQLINK. THE CUSTOMER ATTEMPTED TO ISSUE A NARCOTIC THAT REQUIRES AN RXVERIFY CODE. 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 25135906 ↗MalfunctionJun 30, 2025Failure to Eject; Failure to Eject
IT WAS REPORTED BY THE CUSTOMER THAT BD PYXIS¿ MEDBANK MINI AUX WAS NOT ABLE TO PULL HYDROCHLOROTHIAZIDE (HCTZ) 25 MG TAB IN PROFILE, DESPITE USING OVERRIDE FUNCTION. PROFILE AMOUNT IS SET TO 0.5 AND SHOULD BE A WHOLE NUMBER. USER WILL CONTACTED THE PHARMACY FOR ASSISTANCE ON THAT MED ORDER. THERE WERE NO ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS INCIDENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22354307 ↗
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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