BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ZOOM CRITICAL CARE BED

    MDR report key: 2022035 · Received March 10, 2011

    Report

    Report Number
    1831750-2011-02380
    Event Type
    Malfunction
    Date Received
    March 10, 2011
    Date of Event
    January 21, 2011
    Report Date
    January 21, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OR, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    CONCLUSION: INVESTIGATION IS STILL IN PROCESS.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT ALLEGEDLY, THE TRANSFORMER IS BURNING. IT IS UNK IF THERE WAS PT INVOLVEMENT OR IF THERE ARE ADVERSE CONSEQUENCES TO REPORT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ZOOM CRITICAL CARE BED A/C POWERED HOSPITAL BED FNL STRYKER MEDICAL 2040 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK