BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    IN TOUCH ZU

    MDR report key: 1974064 · Received December 28, 2010

    Report

    Report Number
    1831750-2010-05219
    Event Type
    Malfunction
    Date Received
    December 28, 2010
    Date of Event
    December 6, 2010
    Report Date
    December 6, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    LEFT FOOT END SIDERAIL.

    Description of Event or Problem · 1

    IT WAS REPORTED VIA FIELD TECHNICIAN, (B)(6), THAT THE PRODUCT SUFFERED DAMAGE WHEN A CT SCAN TABLE WAS LOWERED ONTO THE LEFT FOOT END SIDERAIL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 IN TOUCH ZU AC POWERED HOSPITAL BED FNL STRYKER CORP., MEDICAL DIV. 2141 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK