BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PROCEDURAL STRETCHER

    MDR report key: 22194987 · Received June 12, 2025

    Report

    Report Number
    3006697241-2025-00185
    Event Type
    Malfunction
    Date Received
    June 12, 2025
    Date of Event
    May 29, 2025
    Report Date
    June 12, 2025
    Manufacturer
    BAXTER HEALTHCARE CORPORATION
    Product Code
    FPO
    UDI-DI
    00887761000957
    PMA / PMN Number
    K922809
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IN, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 0

    HILLROM RECEIVED A REPORT FROM A CUSTOMER THROUGH MW 5170302 OF A POWER CORD DAMAGE WITH EXPOSED COPPER WIRES. THERE WAS NO PATIENT/USER INJURY REPORTED. CUSTOMER INFORMATION, DEVICE MODEL OR SERIAL NUMBER WERE NOT PROVIDED. BAXTER HAS CAPTURED THIS REPORTED EVENT UNDER GENERIC STRETCHER BED. AS NO SERIAL NUMBER WAS PROVIDED FOR THIS BED, A SEARCH OF THE HILLROM MAINTENANCE RECORDS FOR ANY HILLROM PERFORMED PREVENTATIVE MAINTENANCE ON THIS BED WAS UNABLE TO BE COMPLETED. IT IS UNKNOWN IF THE FACILITY PERFORMS PREVENTATIVE MAINTENANCE ON THEIR BEDS. NO FURTHER INFORMATION IS AVAILABLE ON THE REPORTED EVENT OF THE BED AT THIS TIME. IF ANY ADDITIONAL RELEVANT INFORMATION IS IDENTIFIED, THE ADDITIONAL RELEVANT INFORMATION WILL BE SUBMITTED IN A SUPPLEMENTAL REPORT.

    Description of Event or Problem · 0

    BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN STATING THE POWER CORD HAD DAMAGE WITH EXPOSED COPPER WIRES. THERE WAS NO PATIENT/USER INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2013568 PROCEDURAL STRETCHER STRETCHER, WHEELED FPO BAXTER HEALTHCARE CORPORATION P8000 00887761000957

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown