BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    IN TOUCH EU

    MDR report key: 2971968 · Received January 21, 2013

    Report

    Report Number
    1831750-2013-90508
    Event Type
    Malfunction
    Date Received
    January 21, 2013
    Date of Event
    December 22, 2012
    Report Date
    December 22, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE REASON FOR THE SERIALIZATION STARTING WITH (B)(4) IS TO PROVIDE CLARIFICATION FOLLOWING A CHANGE IN STRYKER'S ELECTRONIC COMPLAINT SYSTEMS.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE FOOTBOARD HAD INTERMITTENT POWER ALONG WITH PLASTIC DEBRIS OBSTRUCTING THE CONNECTION. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    28938 IN TOUCH EU A/C HOSPITAL BED FNL STRYKER MEDICAL 2131 NA

    Patients

    Seq Age Sex Outcome Treatment
    1