BEUDAMED
    FDA Adverse Event Other Summary report: N

    PENUMBRA SYSTEM REPERFUSION CATHETER 032

    MDR report key: 1931352 · Received December 13, 2010

    Report

    Report Number
    MW5018597
    Event Type
    Other
    Date Received
    December 13, 2010
    Report Date
    December 13, 2010
    Manufacturer
    PENUMBRA
    Product Code
    NRY
    Report Source
    Voluntary report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    RECALL NOTICE SENT OUT... RECALL PRODUCT NOT FOUND IN DEPT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PENUMBRA SYSTEM REPERFUSION CATHETER 032 PENUMBRA SYSTEM REPERFUSION CATHETER 032 NRY PENUMBRA F15020

    Patients

    Seq Age Sex Outcome Treatment
    1