BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECHRIST DUAL HT.HYD.STRETCHER

    MDR report key: 1933115 · Received December 13, 2010

    Report

    Report Number
    1831750-2010-04770
    Event Type
    Malfunction
    Date Received
    December 13, 2010
    Date of Event
    November 16, 2010
    Report Date
    November 16, 2010
    Manufacturer
    STRYKER CORP, MEDICAL DIVISION
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    WHEN THE SERVICE TECH ARRIVED TO FACILITY TO ACCESS THE DEVICE, THE DEVICE HAD ALREADY BEEN REPAIRED BY HOSP MAINTENANCE. UNABLE TO DETERMINE HOW MANY RIVETS WERE BROKEN AND REPLACED OR THE RISK SEVERITY.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE RIVETS WERE BROKEN OFF THE FOWLER. NO ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SECHRIST DUAL HT.HYD.STRETCHER HOSPITAL WHEELED STRETCHER FPO STRYKER CORP, MEDICAL DIVISION 0721560000 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK