FDA Adverse Event Malfunction Summary report: N

BD PYXIS¿ MEDBANK TOWER

MDR report key: 25040193 · Received April 30, 2026

Report

Report Number
2016493-2026-24906
Event Type
Malfunction
Date Received
April 30, 2026
Date of Event
April 2, 2026
Report Date
April 7, 2026
Manufacturer
CAREFUSION 303, INC.
Product Code
BRY
UDI-DI
10885403517167
PMA / PMN Number
EXEMPT
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
VA, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

A REVIEW OF THE COMPLAINT HISTORY FOR SN (B)(6) WAS PERFORMED IN SALESFORCE WHICH DID NOT LOCATE SIMILAR COMPLAINT(S) WITH THE SAME FAILURE MODE FOR THIS SERIAL NUMBER. A REVIEW OF THE DEVICE HISTORY RECORD FOR SN (B)(6) WAS PERFORMED FROM THE DATE OF MANUFACTURE, 02-JAN-2024 AND CONFIRMED THAT THIS DEVICE WAS NOT PREVIOUSLY RETURNED FOR SERVICING AND THERE WERE NO PRODUCTION FAILURES WHICH CORRELATES TO THE CUSTOMER REPORTED ISSUE. UPON INVESTIGATION OF THIS INCIDENT, IT WAS FOUND THAT THE CABINET WAS OFF BECAUSE THE UNINTERRUPTED POWER SUPPLY (UPS) BOX WAS TURNED OFF. A TECHNICAL SUPPORT SPECIALIST (TSS) MENTIONED THAT THE CUSTOMER FOUND ALL IN ONE (AIO) POWER BUTTON AND TURNED IT ON AND AFTER THE CUBEX APPLICATION WAS LAUNCHED. THE USER COULD ISSUE THE ITEM SUCCESSFULLY. THE SYSTEM FUNCTIONED AS INTENDED AFTER THE TECHNICAL SUPPORT SPECIALIST INVESTIGATED THE INCIDENT.

Description of Event or Problem · 0

IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ MEDBANK TOWER, THE CABINET WAS DOWN AND MEDICATION COULD NOT BE ISSUED. THE CUSTOMER WAS UNABLE TO ISSUE AMOX/CLAV 875/125 MG TABLET. THE CUSTOMER REPORTED THAT A MALFUNCTION TOOK PLACE WHEN THE USER TRIED TO DISPENSE MEDICATION TO THE PATIENT. THERE WERE NO DELAY OR ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
190109 BD PYXIS¿ MEDBANK TOWER AUTOMATED DISPENSING CABINET BRY CAREFUSION 303, INC. 500004500000 10885403517167

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown