BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SARNS STERNAL SAW II

    MDR report key: 87446 · Received April 29, 1997

    Report

    Report Number
    1828100-1997-00010
    Event Type
    Injury
    Date Received
    April 29, 1997
    Date of Event
    April 9, 1997
    Report Date
    April 29, 1997
    Manufacturer
    3M HEALTH CARE SARNS AND CDI PRODUCTS
    Product Code
    DWH
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    DURING SURGERY, A SCREW CAME OUT OF THE TOP OF THE STERNAL SAW AND FELL INTO THE THORACIC CAVITY. THE SCREW WAS RETRIEVED WITH INCIDENT. NO PATIENT INJURY OR COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS INCIDENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SARNS STERNAL SAW II STERNAL SAW DWH 3M HEALTH CARE SARNS AND CDI PRODUCTS 98-0702-0597-0 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Required Intervention