BEUDAMED
    FDA Adverse Event Injury Summary report: N

    3.0 X 14MM VAL SCREW, TI

    MDR report key: 17563008 · Received August 17, 2023

    Report

    Report Number
    1220246-2023-07520
    Event Type
    Injury
    Date Received
    August 17, 2023
    Date of Event
    August 7, 2018
    Report Date
    December 13, 2024
    Manufacturer
    ARTHREX, INC.
    Product Code
    HWC
    UDI-DI
    00888867050228
    PMA / PMN Number
    K143614
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    501

    Narratives

    Additional Manufacturer Narrative · 0

    THE CONTRIBUTION OF THE DEVICE TO THE REPORTED EVENT COULD NOT BE DETERMINED, AS THE DEVICE WAS NOT RETURNED FOR EVALUATION. THE ROOT CAUSE OF THE EVENT COULD NOT BE DETERMINED, FROM THE INFORMATION AVAILABLE AND WITHOUT DEVICE EVALUATION. IF THE DEVICE BECOMES AVAILABLE FOR EVALUATION, A FOLLOW-UP REPORT WILL BE SUBMITTED.

    Additional Manufacturer Narrative · 0

    ADDITIONAL INFORMATION: G3, H3, H6. BASED ON THE INFORMATION PROVIDED WHICH MAY INCLUDE THE DEVICE (IF AVAILABLE AND RETURNED), PICTURES, VIDEOS, EVENT DESCRIPTION, AND ANY ADDITIONAL INFORMATION FROM THE FIELD, ARTHREX WAS ABLE TO CONCLUDE A MOST LIKELY CAUSE. THE MOST LIKELY CAUSE FOR THE REPORTED FAILURE CAN BE ATTRIBUTED TO A PATIENT-SPECIFIC EVENT.

    Description of Event or Problem · 0

    IT WAS REPORTED, THAT THE PATIENT UNDERWENT SURGERY ON (B)(6) 2018. FOR AN OPEN REDUCTION INTERNAL FIXATION OF A LEFT TRIMALLEOLAR ANKLE FRACTURE, WITH FIXATION OF THE DISTAL FIBULA FRACTURE, POSTERIOR MALLEOLUS FRACTURE, AND SYNDESMOTIC FIXATION. DURING THE (B)(6) 2018 SURGERY, THE FOLLOWING PRODUCTS WERE USED AND/OR IMPLANTED: AR-8740-52PTS, QCKFIX SCRW, TI, CANN ST, CANC.,4.0X 52MM, LOT/SERIAL#: (B)(6); AR-8925T K-LESS, T-ROPE W/DRV, SYN REPR, TI, LOT/SERIAL#: (B)(6); AR-8933-20, LO-PRO SCRW, TI, 3.0MMX 20MMCORT, LOT/SERIAL#: (B)(6); AR-8933V-12, 3.0 X 12MM VAL SCREW, TI, LOT/SERIAL#: (B)(6); AR-8933V-14, 3.0 X 14MM VAL SCREW, TI, LOT/SERIAL#: (B)(6); AR-8933V-16, 3.0 X 16MM VAL SCREW, TI, LOT/SERIAL#: (B)(6); AR-8933V-18, 3.0 X 18MM VAL SCREW, TI, LOT/SERIAL#: (B)(6); AR-8933V-20, 3.0 X 20MM VAL SCREW, TI, LOT/SERIAL#: (B)(6); AR-8935-12, LO-PRO SCRW, TI, 3.5MMX 12MM, LOT/SERIAL#: (B)(6); AR-8935-14, LO-PRO SCRW, TI, 3.5MMX 14MM, LOT/SERIAL#: (B)(6); AR-8935-14, LO-PRO SCRW, TI, 3.5MMX 14MM, LOT/SERIAL#: (B)(6); AR-8935-26, LO-PRO SCRW, TI, 3.5MMX 26MM, LOT/SERIAL#: (B)(6); AR-8943-01, GUIDE WIRE, TROCAR TIP, 1.35 MM, LOT/SERIAL#: (B)(6); AR-8943-02, DRILL BIT, CANNULATED, 2.6MM, LOT/SERIAL#: (B)(6); AR-8943-16, 2.0MM DRILL BIT, CALIBRATED, LOT/SERIAL#: (B)(6); AR-8943-30 ,2.5MM DRILL BIT, LOT/SERIAL#: (B)(6); AR-8943-42, 2.5MM DRILL BIT, CALIBRATED, LOT/SERIAL#: (B)(6); AR-9943BL-04, LOCKING DISTAL FIBULA PLATE, TI, LEFT,4H, LOT/SERIAL#: (B)(6). AFTER SURGERY, IT WAS REPORTED, THE PATIENT BEGAN TO EXPERIENCE ALLERGY LIKE SYMPTOMS AND ON (B)(6) 2018. A REVISION WAS PERFORMED BY THE SAME SURGEON AND THE ARTHREX DEVICES WERE REMOVED. INCLUDING THE AR-9943BL-04 (LOT (B)(6)) AND THE AR-8925T (LOT (B)(6)).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1738115 3.0 X 14MM VAL SCREW, TI BONE FIXATION SCREW/PLATE HWC ARTHREX, INC. 3.0 X 14MM VAL SCREW, TI 031809 00888867050228

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Other