FDA Adverse Event Malfunction Summary report: N

BD PYXIS¿ MEDBANK TOWER AUX

MDR report key: 23520672 · Received November 11, 2025

Report

Report Number
2016493-2025-132903
Event Type
Malfunction
Date Received
November 11, 2025
Date of Event
October 14, 2025
Report Date
October 19, 2025
Manufacturer
CAREFUSION 303, INC.
Product Code
BRY
PMA / PMN Number
EXEMPT
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

UPON INVESTIGATION OF THE ACTUAL DEVICE USED IN THIS INCIDENT, IT WAS DETERMINED THAT THE MEDICATION DATA FAILED TO APPEAR ON THE PATIENT'S PROFILE. A TECHNICAL SUPPORT SPECIALIST (TSS) LOGGED INTO MED BANK (MYQ) LINK TO INVESTIGATE AND IDENTIFIED THAT THE MEDICATIONS IN QUESTION WERE NOT CURRENTLY STOCKED IN THE CABINET. THE TSS EXPLAINED THE CUSTOMER THAT THE MEDICATIONS NOT STOCKED IN THE CABINET WOULD NOT APPEAR ON THE PATIENT'S PROFILE, WHICH CLARIFIED THE ISSUE. THE SYSTEM FUNCTIONED AS INTENDED AFTER THE TECHNICAL SUPPORT SPECIALIST INVESTIGATED THE DEVICE. D4 & H4: SERIAL NUMBER, UNIQUE DEVICE IDENTIFIER AND MANUFACTURER DATE NOT AVAILABLE.

Description of Event or Problem · 0

IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ MEDBANK TOWER AUX HAD MEDS THAT WERE NOT STOCKED ON THE CABINET WILL NOT SHOW ON THE PATIENT'S PROFILE. 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
1878463 BD PYXIS¿ MEDBANK TOWER AUX AUTOMATED DISPENSING CABINET BRY CAREFUSION 303, INC. 500004500001

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown