BEUDAMED
    FDA Adverse Event Injury Summary report: N

    RENAISSANCE 29 P-WASH

    MDR report key: 1754789 · Received July 9, 2010

    Report

    Report Number
    1831750-2010-01477
    Event Type
    Injury
    Date Received
    July 9, 2010
    Date of Event
    June 5, 2010
    Report Date
    July 1, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIVISION
    Product Code
    FPO
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT A FEMALE PT WAS ADJUSTING HERSELF WHILE ON THE STRETCHER AND RUPTURED A TENDON ON THE 3RD FINGER OF HER LEFT HAND AFTER IT GOT CAUGHT IN A RESTRAINT SLOT ON THE SIDE OF THE STRETCHER. THERE IS A POSSIBILITY THAT SHE MAY HAVE TO HAVE SURGERY TO CORRECT THE ISSUE. THE FINGER IS CURRENTLY IN A SPLINT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RENAISSANCE 29 P-WASH HOSPITAL WHEELED STRETCHER FPO STRYKER CORP., MEDICAL DIVISION 1731

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK Required Intervention