BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    RENAISSANCE 26 P-WASS 10/04

    MDR report key: 2933648 · Received January 29, 2013

    Report

    Report Number
    0001831750-2013-00500
    Event Type
    Malfunction
    Date Received
    January 29, 2013
    Date of Event
    January 8, 2013
    Report Date
    January 8, 2013
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE SIDERAIL WOULD NO LONGER LATCH IN THE UPRIGHT POSITION DUE TO A BROKEN WELD.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    39203 RENAISSANCE 26 P-WASS 10/04 STRETCHER, WHEELED FPO STRYKER MEDICAL-KALAMAZOO 1231

    Patients

    Seq Age Sex Outcome Treatment
    1