BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    RENAISSANCE 26 P-WASS

    MDR report key: 1974655 · Received December 29, 2010

    Report

    Report Number
    1831750-2010-05301
    Event Type
    Malfunction
    Date Received
    December 29, 2010
    Date of Event
    December 2, 2010
    Report Date
    December 2, 2010
    Manufacturer
    STRYKER MEDICAL KALAMAZOO
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE FOOT RIGHT LATCH SPINDLE BASE WELD IS BROKEN. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RENAISSANCE 26 P-WASS HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL KALAMAZOO 1231

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK