FDA Adverse Event Malfunction Summary report: N

BD PYXIS¿ ES SERVER

MDR report key: 25108759 · Received May 7, 2026

Report

Report Number
2016493-2026-26517
Event Type
Malfunction
Date Received
May 7, 2026
Date of Event
April 8, 2026
Report Date
April 14, 2026
Manufacturer
CAREFUSION 303, INC.
Product Code
BRY
PMA / PMN Number
EXEMPT
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TC
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

D.4 & H.4: SERIAL NUMBER, UNIQUE DEVICE IDENTIFIER, AND MANUFACTURER DATE NOT AVAILABLE. UPON INVESTIGATION OF THE ACTUAL DEVICE USED IN THIS INCIDENT, IT WAS DETERMINED THAT THE MEDICAL RECORD NUMBER NOT SHOWN IN PYXIS AND MESSAGE NOT CROSSING. A TECHNICAL SUPPORT SPECIALIST (TSS) DETERMINED THAT THE ISSUE WAS CAUSED BY A MISSING "M" IN THE HL7 MESSAGE HEADER (MSH) FOR ADMIT DISCHARGE TRANSFER AND RDE MESSAGES. INVESTIGATION CONFIRMED THAT THE HIS SENT COMPLETE MESSAGES, BUT THE PYXIS INTERFACE SERVER INTERMITTENTLY RECEIVED THEM WITH THE HEADER MISSING. THE ISSUE WAS RESOLVED BY RESTARTING THE PYXIS-HIS INTERFACE, AFTER WHICH MESSAGES WERE RECEIVED CORRECTLY. THE CUSTOMER CONFIRMED RESOLUTION AND AGREED TO CLOSE THE CASE. THE SYSTEM FUNCTIONED AS INTENDED AFTER THE TECHNICAL SUPPORT SPECIALIST TROUBLESHOT THE DEVICE.

Description of Event or Problem · 0

IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ ES SERVER, THE MRN WAS NOT APPEARING IN PYXIS. THE CUSTOMER REPORTED THAT MESSAGES WERE NOT CROSSING OVER TO THE PYXIS CONSOLE SERVER, WITH THE ERROR MESSAGE: "NO MAPPING DEFINED, DROPPING MESSAGE. HOWEVER, THERE WERE NO DELAYS OR ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
344459 BD PYXIS¿ ES SERVER AUTOMATED DISPENSING CABINET BRY CAREFUSION 303, INC.

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown SN: (B)(6), LOCATION: SERVER ROOM.