BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    RECOVERY ROOM STRETCH

    MDR report key: 2933480 · Received December 21, 2012

    Report

    Report Number
    1831750-2012-13223
    Event Type
    Malfunction
    Date Received
    December 21, 2012
    Date of Event
    November 26, 2012
    Report Date
    November 26, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE HEAD END JACK COULD NOT BE RAISED. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RECOVERY ROOM STRETCH HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 1510 NA

    Patients

    Seq Age Sex Outcome Treatment
    1