BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BD PYXIS¿ ANESTHESIA STATION ES

    MDR report key: 23034613 · Received September 11, 2025

    Report

    Report Number
    2016493-2025-113272
    Event Type
    Malfunction
    Date Received
    September 11, 2025
    Date of Event
    August 17, 2025
    Report Date
    October 22, 2025
    Manufacturer
    CAREFUSION 303, INC.
    Product Code
    BRY
    UDI-DI
    10885403477836
    PMA / PMN Number
    EXEMPT
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CO, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    CORRECTION : UPON FURTHER REVIEW, IT WAS DETERMINED THAT THIS REPORT WAS INADVERTENTLY SUBMITTED AS A DUPLICATE OF MFR. REPORT NUMBER 2016493-2025-113272 PLEASE REFER TO MFR. REPORT NUMBER 2016493-2025-113764.

    Additional Manufacturer Narrative · 0

    A DEVICE EVALUATION IS ANTICIPATED, BUT HAS NOT YET BEGUN. UPON COMPLETION OF THE INVESTIGATION, A SUPPLEMENTAL REPORT WILL BE FILED.

    Description of Event or Problem · 0

    IT WAS REPORTED BY THE CUSTOMER THAT A BD PYXIS¿ ANESTHESIA STATION ES HAD A DRAWER CONNECTION WAS FAILED TO RECOVER. THE CUSTOMER STATED THAT THE MALFUNCTION OCCURRED WHILE USER TRIED TO ISSUE MEDICATION TO A PATIENT AND THERE WAS A DELAY IN DISPENSING MEDICATION TO A PATIENT. THERE WERE NO ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2305809 BD PYXIS¿ ANESTHESIA STATION ES AUTOMATED DISPENSING CABINET BRY CAREFUSION 303, INC. 500400001500 10885403477836

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown