BEUDAMED
    FDA Adverse Event Summary report: N

    SM104 MSERIES W5TH WHLOBS3/07

    MDR report key: 1081903 · Received July 25, 2008

    Report

    Report Number
    1831750-2008-00101
    Date Received
    July 25, 2008
    Date of Event
    June 29, 2008
    Report Date
    June 29, 2008
    Manufacturer
    STRYKER CORP - MEDICAL DIV
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE BRAKE RINGS WERE DAMAGED DUE TO LIKELY CUSTOMER ABUSE. USER ERROR CONTRIBUTED TO BRAKE RING DAMAGE.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE BRAKES WERE NOT HOLDING AS A RESULT OF DAMAGED BRAKE RINGS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SM104 MSERIES W5TH WHLOBS3/07 STRETCHER FPO STRYKER CORP - MEDICAL DIV 1005

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK