BEUDAMED
    FDA Adverse Event Injury Summary report: N

    TEBBETTS FIBEROPTIC SS RETRACTOR

    MDR report key: 1252163 · Received November 25, 2008

    Report

    Report Number
    1423507-2008-00094
    Event Type
    Injury
    Date Received
    November 25, 2008
    Report Date
    November 25, 2008
    Manufacturer
    CARDINAL HEALTH
    Product Code
    GAD
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE DEVICE HAS NOT ARRIVED FOR EVAL YET AND THE LOT NUMBER WAS NOT PROVIDED. WITHOUT THE LOT NUMBER, THE DEVICE HISTORY COULD NOT BE REVIEWED. WITHOUT INSTRUMENT, CAUSE FOR FAILURE COULD NOT BE DETERMINED OR THE ISSUE CONFIRMED. WHEN THE PRODUCT ARRIVES, A FOLLOW-UP REPORT WILL BE FILED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TEBBETTS FIBEROPTIC SS RETRACTOR GAD CARDINAL HEALTH 88-1087 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1