BEUDAMED
    FDA Adverse Event Injury Summary report: N

    COMPREHENSIVE REVERSE SHOULDER CENTRAL SCREW

    MDR report key: 6944263 · Received October 12, 2017

    Report

    Report Number
    0001825034-2017-06898
    Event Type
    Injury
    Date Received
    October 12, 2017
    Date of Event
    July 3, 2017
    Report Date
    October 11, 2017
    Manufacturer
    BIOMET ORTHOPEDICS
    Product Code
    KWS
    PMA / PMN Number
    PK132239
    Removal / Correction Number
    N/A
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NJ, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). CONCOMITANT MEDICAL PRODUCTS: COMPREHENSIVE REVERSE SHOULDER GLENOSPHERE, CATALOG#: 115310, LOT#: 988500. COMPREHENSIVE SHOULDER MINI HUMERAL STEM, CATALOG#: 113632, LOT#: 430770. COMPREHENSIVE REVERSE SHOULDER FIXED LOCKING SCREW, CATALOG#: 180551, LOT#: 225090. COMPREHENSIVE REVERSE SHOULDER GLENOSPHERE MINI BASEPLATE, CATALOG#: 010000589, LOT#: 415160. COMPREHENSIVE REVERSE SHOULDER FIXED LOCKING SCREW, CATALOG#: 180552, LOT#: 446170. COMPREHENSIVE REVERSE SHOULDER FIXED LOCKING SCREW, CATALOG#: 180551, LOT#: 870060. COMPREHENSIVE REVERSE SHOULDER FIXED LOCKING SCREW, CATALOG#: 180550, LOT#: 724660. COMPREHENSIVE REVERSE SHOULDER HUMERAL TRAY W LOCKING RING, CATALOG#: 115370, LOT#: 931490. COMPREHENSIVE REVERSE SHOULDER HUMERAL BEARING, CATALOG#: XL-115363, LOT#: 355870. MULTIPLE MDR REPOTS WERE FILLED FOR THIS EVENT: 0001825034-2017-06881, 06896, 06897, 06898, 06899, 08532, 08533, 08534, 08535, 08536. REPORTED EVENT WAS UNABLE TO BE CONFIRMED DUE TO LIMITED INFORMATION RECEIVED FROM THE CUSTOMER. DEVICE HISTORY RECORD (DHR) WAS REVIEWED AND NO DISCREPANCIES WERE FOUND. REVIEW OF THE COMPLAINT HISTORY DETERMINED THAT NO FURTHER ACTION(S) IS/ARE REQUIRED. ROOT CAUSE WAS UNABLE TO BE DETERMINED AS THE NECESSARY INFORMATION TO ADEQUATELY INVESTIGATE THE REPORTED EVENT WAS NOT PROVIDED. IF ANY FURTHER INFORMATION IS FOUND WHICH WOULD CHANGE OR ALTER ANY CONCLUSIONS OR INFORMATION, A SUPPLEMENTAL WILL BE FILED ACCORDINGLY. ZIMMER BIOMET WILL CONTINUE TO MONITOR FOR TRENDS.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT PATIENT UNDERWENT LEFT SHOULDER 2-STAGE REVISION DUE TO INFECTION. NO FURTHER INFORMATION HAS BEEN PROVIDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    723579 COMPREHENSIVE REVERSE SHOULDER CENTRAL SCREW PROSTHESIS, SHOULDER KWS BIOMET ORTHOPEDICS N/A 430530

    Patients

    Seq Age Sex Outcome Treatment
    1 Hospitalization| R