BEUDAMED
    FDA Adverse Event Injury Summary report: N

    GLIDE SYSTEM, LAUNDERABLE

    MDR report key: 2071808 · Received April 21, 2011

    Report

    Report Number
    1831750-2011-03880
    Event Type
    Injury
    Date Received
    April 21, 2011
    Date of Event
    March 24, 2011
    Report Date
    March 24, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THREE GLIDES HAVE HAD THE PATIENT CENTERING STRAPS TORN AT THE SEAMS. THERE WAS PATIENT INVOLVEMENT AND AN ADVERSE EVENT WAS REPORTED WITH THE CAREGIVER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GLIDE SYSTEM, LAUNDERABLE MANUAL PATIENT TRANSFER DEVICE FPO STRYKER MEDICAL 3062 NA

    Patients

    Seq Age Sex Outcome Treatment
    1