BEUDAMED
    FDA Adverse Event Other Summary report: N

    PRIME BIG WHEEL STRETCHER, 30"

    MDR report key: 2592155 · Received May 23, 2012

    Report

    Report Number
    1831750-2012-05607
    Event Type
    Other
    Date Received
    May 23, 2012
    Date of Event
    April 25, 2012
    Report Date
    April 25, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MO, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE CUSTOMER ALLEGED THAT THE JACK WAS DRIFTING; HOWEVER, THE STRYKER TECHNICIAN COULD NOT DUPLICATE THE ISSUE AND ALL OPERATIONS PERFORMED TO SPECIFICATIONS. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PRIME BIG WHEEL STRETCHER, 30" HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 1115000030 NA

    Patients

    Seq Age Sex Outcome Treatment
    1