BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ASPEN SURGICAL PRODUCTS, BARD PARKER BLADES

    MDR report key: 2653223 · Received June 28, 2012

    Report

    Report Number
    1836161-2012-00003
    Event Type
    Malfunction
    Date Received
    June 28, 2012
    Date of Event
    April 25, 2012
    Report Date
    June 28, 2012
    Manufacturer
    ASPEN SURGICAL PRODUCTS
    Product Code
    LRO
    PMA / PMN Number
    EXEMPT
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    NURSE

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ASPEN SURGICAL PRODUCTS, BARD PARKER BLADES BARD PARKER SAFETY BLADE SIZE 10 LRO ASPEN SURGICAL PRODUCTS 373910 0000852

    Patients

    Seq Age Sex Outcome Treatment
    1 *