FDA Adverse Event Malfunction Summary report: N

BD PYXIS¿ ES SERVER

MDR report key: 25240697 · Received May 21, 2026

Report

Report Number
2016493-2026-30888
Event Type
Malfunction
Date Received
May 21, 2026
Date of Event
April 23, 2026
Report Date
April 29, 2026
Manufacturer
CAREFUSION 303, INC.
Product Code
BRY
PMA / PMN Number
EXEMPT
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
KS, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

D4 & H4: SERIAL NUMBER, MODEL, CATALOG, UNIQUE DEVICE IDENTIFIER AND MANUFACTURER DATE NOT AVAILABLE. UPON INVESTIGATION OF THE ACTUAL DEVICE USED IN THIS INCIDENT, IT WAS DETERMINED THAT THE MULTIPLE PATIENTS WERE NOT SHOWING AT MULTIPLE STATIONS. A TECHNICAL SUPPORT SPECIALIST (TSS) DIALED INTO THE SERVER AND RESTARTED THE EXTERNAL MESSAGING SERVICE. THE CAREFUSION COORDINATION ENGINE (CCE) INTERFACE SERVICES UTILITY (BUILD 1) PACKAGE WAS DEPLOYED SUCCESSFULLY. TWO XML FILES WERE FOUND STUCK. TSS ADVISED ASSIGNING THE TICKET TO A PRODUCT SUPPORT ENGINEER (PSE) FOR FURTHER REVIEW. A QUERY WAS RUN TO VERIFY LOCAL DATE AND TIME AND ADMIT DISCHARGE TRANSFER (ADT) AND RDE ORDERS MESSAGES WERE CONFIRMED TO BE CROSSING TO THE ES SERVER THROUGH THE CCE INTERFACE. THE SYSTEM FUNCTIONED AS INTENDED AFTER TECHNICAL SUPPORT SPECIALIST TROUBLESHOT THE DEVICE.

Description of Event or Problem · 0

IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ ES SERVER, MULTIPLE PATIENTS WAS NOT SHOWN AT MULTIPLE STATION. THE CUSTOMER STATED THAT THERE WAS A DELAY IN PATIENT CARE. THERE WERE NO ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
94348 BD PYXIS¿ ES SERVER AUTOMATED DISPENSING CABINET BRY CAREFUSION 303, INC.

Patients

Seq Age Sex Outcome Treatment
1