BEUDAMED
    FDA Adverse Event Injury Summary report: N

    UNK - SCREWS: TRAUMA

    MDR report key: 8910708 · Received August 20, 2019

    Report

    Report Number
    2939274-2019-59955
    Event Type
    Injury
    Date Received
    August 20, 2019
    Report Date
    July 22, 2019
    Manufacturer
    WRIGHTS LANE SYNTHES USA PRODUCTS LLC
    Product Code
    HWC
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 0

    DEPUY SYNTHES IS SUBMITTING THIS REPORT PURSUANT TO THE PROVISIONS OF 21 CFR, PART 803. THIS REPORT MAY BE BASED ON INFORMATION WHICH DEPUY SYNTHES HAS NOT BEEN ABLE TO INVESTIGATE OR VERIFY PRIOR TO THE REQUIRED REPORTING DATE. THIS REPORT DOES NOT REFLECT A CONCLUSION BY FDA, DEPUY SYNTHES OR ITS EMPLOYEES THAT THE REPORT CONSTITUTES AN ADMISSION THAT THE DEVICE, DEPUY SYNTHES, OR ITS EMPLOYEES CAUSED OR CONTRIBUTED TO THE POTENTIAL EVENT DESCRIBED IN THIS REPORT. BASED ON THE INFORMATION AVAILABLE, IT HAS BEEN DETERMINED THAT NO CORRECTIVE AND/OR PREVENTATIVE ACTION IS PROPOSED. THIS COMPLAINT WILL BE ACCOUNTED FOR AND MONITORED VIA POST MARKET SURVEILLANCE ACTIVITIES. IF ADDITIONAL INFORMATION IS MADE AVAILABLE, THE INVESTIGATION WILL BE UPDATED AS APPLICABLE. DEVICE WAS USED FOR TREATMENT, NOT DIAGNOSIS. IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT ON AN UNKNOWN DATE, POSTOPERATIVELY THE PATIENT HAD DELAYED UNION OF ARTHRODESIS REQUIRING BONE STIMULATOR THERAPY. THE PATIENT HAD PRIMARY MEDIAL COLUMN ARTHRODESIS TALONAVICULAR JOINT (TNJ), NAVICULOCUNEIFORM JOINT (NCJ), AND FIRST TARSOMETATARSAL JOINT (TMTJ) PROCEDURE WITH MEDIAL COLUMN FUSION PLATE SYSTEM THAT WAS IMPLANTED ON (B)(6) 2016. SPREADSHEET LISTING PRODUCT PERFORMANCE INFORMATION ON THIRTY-FIVE PATIENTS TREATED WITH THE MEDIAL COLUMN FUSION PLATE 3.5 MM SYSTEM RECEIVED BY THE CLINICAL TEAM. THERE WAS NO REMOVAL/REVISION SURGERY PERFORMED TO THE PATIENT. PATIENT STATUS IS UNKNOWN.

    Additional Manufacturer Narrative · 1

    THIS REPORT IS FOR UNKNOWN SCREWS/UNKNOWN LOT. PART AND LOT NUMBER ARE UNKNOWN. WITHOUT THE SPECIFIC PART NUMBER; THE UDI NUMBER AND 510-K NUMBER IS UNKNOWN. COMPLAINANT PART IS NOT EXPECTED TO BE RETURNED FOR MANUFACTURER REVIEW/INVESTIGATION. (B)(4). WITHOUT A LOT NUMBER THE DEVICE HISTORY RECORDS REVIEW COULD NOT BE COMPLETED. PRODUCT WAS NOT RETURNED. BASED ON THE INFORMATION AVAILABLE, IT HAS BEEN DETERMINED THAT NO CORRECTIVE AND/OR PREVENTATIVE ACTION IS PROPOSED. THIS COMPLAINT WILL BE ACCOUNTED FOR AND MONITORED VIA POST MARKET SURVEILLANCE ACTIVITIES. IF ADDITIONAL INFORMATION IS MADE AVAILABLE, THE INVESTIGATION WILL BE UPDATED AS APPLICABLE. DEVICE WAS USED FOR TREATMENT, NOT DIAGNOSIS. IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT ON AN UNKNOWN DATE, POSTOPERATIVELY THE PATIENT HAD DELAYED UNION OF ARTHRODESIS REQUIRING BONE STIMULATOR THERAPY. THE PATIENT HAD PRIMARY MEDIAL COLUMN ARTHRODESIS TALONAVICULAR JOINT (TNJ), NAVICULOCUNEIFORM JOINT (NCJ), AND FIRST TARSOMETATARSAL JOINT (TMTJ) PROCEDURE WITH MEDIAL COLUMN FUSION PLATE SYSTEM THAT WAS IMPLANTED ON (B)(6) 2016. THERE WAS NO REMOVAL/REVISION SURGERY PERFORMED TO THE PATIENT. PATIENT STATUS IS UNKNOWN. THIS REPORT IS FOR UNKNOWN QUANTITY OF UNKNOWN SCREWS. THIS IS REPORT 2 OF 2 FOR COMPLAINT (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    704144 UNK - SCREWS: TRAUMA SCREW, FIXATION, BONE HWC WRIGHTS LANE SYNTHES USA PRODUCTS LLC

    Patients

    Seq Age Sex Outcome Treatment
    1 61 YR Required Intervention