BEUDAMED
    FDA Adverse Event Injury Summary report: N

    TRANSPORT SERIES OBS10/25/04

    MDR report key: 3933964 · Received July 15, 2014

    Report

    Report Number
    0001831750-2014-03159
    Event Type
    Injury
    Date Received
    July 15, 2014
    Date of Event
    June 13, 2014
    Report Date
    June 20, 2014
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    FPO
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE IV POLE HAD CHROME CHIPPING AND A CAREGIVER INJURED THEIR HAND AS A RESULT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    412348 TRANSPORT SERIES OBS10/25/04 STRETCHER, WHEELED FPO STRYKER MEDICAL-KALAMAZOO

    Patients

    Seq Age Sex Outcome Treatment
    1