BD Pyxis™ SW-SVR-ES-57Recalls & reported problems
Carefusion 303, Inc. · BD Pyxis™ Enterprise Server ES (v5.7) · Class 1
All models of BD Pyxis (26)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
3 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 3
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
3 FDA recall records name this device's 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, 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.
Recalls naming this device
- Dec 3, 2025Class IIOpen, Classified
Due a software issue that may result in equipment not receiving timely updates of patient, medication, or related information from enterprise systems.
Z-1028-2026 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- May 8, 2025Class IIOpen, Classified
During automated dispensing cabinet upgrade/installation/reimaging, component manager was left in installed mode, and if a Microsoft patch is then installed this may lead to an error preventing user access to the dispensing software application, which may lead to delay in access to medications/supplies, and delivery/replenishment of patient specific orders; which may lead to delay in patient care.
Z-2017-2025 · Root cause: Software Design Change · Recall details · FDA record ↗
- May 8, 2025Class IIOpen, Classified
Antivirus software was not consistently installed on impacted devices during the implementation process.
Z-2477-2025 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
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
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- 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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