BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    S3 EX - 3005

    MDR report key: 2914902 · Received December 7, 2012

    Report

    Report Number
    1831750-2012-12704
    Event Type
    Malfunction
    Date Received
    December 7, 2012
    Date of Event
    November 28, 2012
    Report Date
    November 28, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    LA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    RETAINING CLIP. THE ISSUE WAS RESOLVED FOR THE CUSTOMER BY THE SERVICE TECH ATTACHING THE RETAINING CLIP ON THE SIDERAIL.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE SIDE RAIL WOULD NOT LOCK INTO PLACE DUE TO THE RETAINING CLIP FOR THE GUIDE PIN NOT BEING ATTACHED. THERE WAS PT INVOLVEMENT; HOWEVER, NO ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 S3 EX - 3005 A/C POWERED HOSPITAL BED FNL STRYKER MEDICAL 3005S3EX NA

    Patients

    Seq Age Sex Outcome Treatment
    1