BEUDAMED
    FDA Adverse Event Injury Summary report: N

    TI LOCK-SCR CANCLS 6.5X25MM

    MDR report key: 7363386 · Received March 22, 2018

    Report

    Report Number
    0001825034-2018-02000
    Event Type
    Injury
    Date Received
    March 22, 2018
    Date of Event
    October 27, 2017
    Report Date
    March 23, 2018
    Manufacturer
    ZIMMER BIOMET, INC.
    Product Code
    LPH
    PMA / PMN Number
    PK991807
    Removal / Correction Number
    N/A
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). ADDITIONAL CONCOMITANT MEDICAL PRODUCTS: PM158036, JONES LT TRFNG SZ 26 HA W POST, 417450; UNKNOWN, UNKNOWN LINER, UNKNOWN; CP161940, TI LOCK-SCR CANCLS 6.5X15MM, 388730; CP161941, TI LOCK-SCR CANCLS 6.5X20MM, 683480; CP161942, TI LOCK-SCR CANCLS 6.5X25MM, 683500; CP161945, TI LOCK-SCR CANCLS 6.5X40MM, 683530; CP161947, TI LOCK-SCR CANCLS 6.5X50MM, 756760; CP161944, TI LOCK-SCR CANCLS 6.5X35MM, UNKNOWN; UNKNOWN, UNKNOWN HEAD, UNKNOWN; UNKNOWN, UNKNOWN STEM, UNKNOWN; CP161943, TI LOCK-SCR CANCLS 6.5X30MM, 683510; CP462153, CUS 9.5MM DRL GD, 463760; CP462154, CUS 9.5MM DRL GD INSTERTER, 464350; CP161945, TI LOCK-SCR CANCLS 6.5X40MM, 683530; CP161943, TI LOCK-SCR CANCLS 6.5X30MM, 683510; CP161943, TI LOCK-SCR CANCLS 6.5X30MM, 683510; CP161943, TI LOCK-SCR CANCLS 6.5X30MM, 683510; CP161942, TI LOCK-SCR CANCLS 6.5X25MM, 683500; CP161942, TI LOCK-SCR CANCLS 6.5X25MM, 725760; CP161942, TI LOCK-SCR CANCLS 6.5X25MM, 725760; CP161942, TI LOCK-SCR CANCLS 6.5X25MM, 725760; CP161942, TI LOCK-SCR CANCLS 6.5X25MM, 725760; CP161942, TI LOCK-SCR CANCLS 6.5X25MM, 725760; CP161941, TI LOCK-SCR CANCLS 6.5X20MM, 683480; CP161941, TI LOCK-SCR CANCLS 6.5X20MM, 683480; CP161941, TI LOCK-SCR CANCLS 6.5X20MM, 683480. (B)(6). REPORTED EVENT WAS UNABLE TO BE CONFIRMED DUE TO LIMITED INFORMATION RECEIVED FROM THE CUSTOMER. DHR WAS REVIEWED AND NO DISCREPANCIES WERE FOUND. REVIEW OF THE COMPLAINT HISTORY DETERMINED THAT NO FURTHER ACTION IS REQUIRED AS NO WERE TRENDS IDENTIFIED. 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. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001825034 - 2017 - 10227, 0001825034 - 2017 - 10222, 0001825034 - 2017 - 10223, 0001825034 - 2017 - 10224, 0001825034 - 2017 - 10225, 0001825034 - 2017 - 10221, 0001825034 - 2017 - 10228, 0001825034 - 2017 - 10229, 0001825034 - 2017 - 10230, 0001825034 - 2017 - 10231, 0001825034 - 2017 - 10232, 0001825034 - 2018 - 01995, 0001825034 - 2018 - 01996, 0001825034 - 2018 - 01997, 0001825034 - 2018 - 01998, 0001825034 - 2018 - 01999, 0001825034 - 2018 - 02001, 0001825034 - 2018 - 02002, 0001825034 - 2018 - 02003, 0001825034 - 2018 - 02004, 0001825034 - 2018 - 02005, 0001825034 - 2018 - 02006, 0001825034 - 2018 - 02007, 0001825034 - 2018 - 02008.

    Additional Manufacturer Narrative · 1

    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 THE PATIENT WAS REVISED TO ADDRESS INFECTION. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN MADE AVAILABLE AT THIS TIME.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    205432 TI LOCK-SCR CANCLS 6.5X25MM PROSTHESIS, HIP LPH ZIMMER BIOMET, INC. N/A 683500

    Patients

    Seq Age Sex Outcome Treatment
    1 Hospitalization| O