BEUDAMED
    FDA Adverse Event Other Summary report: N

    IMPACT

    MDR report key: 2090851 · Received May 2, 2011

    Report

    Report Number
    2242630-2011-00031
    Event Type
    Other
    Date Received
    May 2, 2011
    Report Date
    April 9, 2011
    Manufacturer
    IMPACT INSTRUMENTATION, INC.
    Product Code
    BTA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    DATE NOTIFIED: (B)(6) 2011. A MODEL 321 PORTABLE ASPIRATOR (S/N (B)(4)) FAILED TO OPERATE. AN INSPECTION OF THE DEVICE REVEALED A DEFECTIVE BATTERY PACK AND SWITCH. THE BATTERY PACK AND THE SWITCH WERE REPLACED, THE DEVICE WAS TESTED TO SPECS AND RETURNED TO THE CUSTOMER. NO DEATH OR INJURY RESULTED FROM THE DEVICE MALFUNCTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 IMPACT PORTABLE ASPIRATOR BTA IMPACT INSTRUMENTATION, INC. 321

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Other