BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    NON AC-POWERED PATIENT LIFT

    MDR report key: 3256869 · Received July 31, 2013

    Report

    Report Number
    1525712-2013-06332
    Event Type
    Malfunction
    Date Received
    July 31, 2013
    Report Date
    July 16, 2013
    Manufacturer
    INVACARE TAYLOR STREET
    Product Code
    FNG
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4) - FOLLOW UP #001. INITIAL (B)(4) ISSUED MFR. REPORT # 1525712-2013-06332 INDICTING THE BRAND NAME AS AC POWERED LIFT WITH A COMMON DEVICE NAME OF 880.5500. THE CORRECT BRAND NAME IS NON-AC POWERED PATIENT LIFT WITH A COMMON DEVICE NAME OF 880.5510.

    Description of Event or Problem · 1

    IT WAS REPORTED THE CROSS SUPPORT ON THE RPA600 POWERED LIFT IS BENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    357562 NON AC-POWERED PATIENT LIFT 880.5510 FNG INVACARE TAYLOR STREET RPA600

    Patients

    Seq Age Sex Outcome Treatment
    1 Other