BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MINIBUNION NONLCKNG SCR 2.7MMX14MM STER

    MDR report key: 16991247 · Received May 24, 2023

    Report

    Report Number
    3020584246-2023-00003
    Event Type
    Injury
    Date Received
    May 24, 2023
    Date of Event
    May 3, 2023
    Manufacturer
    SYNTHES TRAUMA : CROSSROADS EXTREMITY SYSTEMS, LLC
    Product Code
    HRS
    UDI-DI
    00815432027019
    PMA / PMN Number
    K181872
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NJ, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    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. IF THE INFORMATION IS UNKNOWN, NOT AVAILABLE OR DOES NOT APPLY, THE SECTION/FIELD OF THE FORM IS LEFT BLANK. H1 ADDITIONAL NARRATIVE: H4, H6: PART: 3100-2714NL LOT: 400290 SUPPLIER: (B)(4). RELEASE TO WAREHOUSE DATE: (B)(4) 2021 A MANUFACTURING RECORD EVALUATION WAS PERFORMED FOR THE FINISHED ARTICLE LOT AND NO NON-CONFORMANCES WERE IDENTIFIED. NOTE: FOLLOWING INVESTIGATION WAS PERFORMED BY CROSSROADS EXTREMITY SYSTEMS. THE PHOTO WAS RETURNED TO DEPUY SYNTHES FOR EVALUATION. THE DEPUY SYNTHES TEAM FORWARDED THE PHOTO TO CROSSROADS EXTREMITY SYSTEMS WHICH CONDUCTED A VISUAL INSPECTION OF THE DEVICE FROM THE RECEIVED IMAGE(S). VISUAL ANALYSIS OF THE RETURNED SAMPLE WAS PERFORMED ON THE MINIBUNION NONLCKNG SCR 2.7MMX14MM STER. THE SUPPLIER LOT HISTORY RECORDS FOR THE PART NUMBER 3100-2714NL AND LOT NUMBER 400290 WERE REVIEWED. LHRS INCLUDED IMPLANT PRINTS SPECIFICATION, QUALITY INSPECTION REPORTS, PROCESS CERTIFICATION , CERTIFICATE OF TEST FOR TITANIUM INGOT, AND SUPPLIER CERTIFICATES OF CONFORMANCE. NON-CONFORMANCES WERE NOT IDENTIFIED BASED ON THE LOTS THAT WOULD LEAD TO THIS EVENT. HENCE, THE COMPLAINT CONDITION WAS NOT CONFIRMED. PROMINENCE LEADING TO IRRITATION IS KNOWN RISK INCLUDED IN THE IFU: ¿OVER TIME, IMPLANTS MAY LOOSEN, FRACTURE, OR CAUSE PAIN AFTER SOFT TISSUE IS HEALED. REMOVAL OF IMPLANTS IS AT THE SURGEON¿S DISCRETION, AND THE APPROPRIATENESS OF THE SELECTED PROCEDURE WILL BE BASED ON THE SURGEON¿S PERSONAL MEDICAL TRAINING AND EXPERIENCE. IT IS IMPERATIVE THAT ADEQUATE POST-OPERATIVE CARE AND PROTECTION BE PROVIDED BY THE SURGEON.¿ THE DIMENSIONAL INSPECTION WAS NOT PERFORMED SINCE THE DEVICE WAS NOT RETURNED. AS PART OF DEPUY SYNTHES QUALITY PROCESS, ALL DEVICES ARE MANUFACTURED, INSPECTED, AND RELEASED TO APPROVED SPECIFICATIONS. THE OVERALL COMPLAINT WAS NOT CONFIRMED FOR THE MINIBUNION NONLCKNG SCR 2.7MMX14MM STER. THERE IS NO INDICATION THAT A DESIGN OR MANUFACTURING ISSUE HAS CAUSED THE COMPLAINT CONDITION AND HENCE THE ROOT CAUSE CANNOT BE DETERMINED. BASED ON THE INVESTIGATION FINDINGS, IT HAS BEEN DETERMINED THAT NO CORRECTIVE AND/OR PREVENTATIVE ACTION IS PROPOSED. ADDITIONAL MONITORING FOR ANY POTENTIAL SAFETY SIGNALS WILL BE CONDUCTED THROUGH COMPLAINT TRENDING AND OTHER POST-MARKET SAFETY SURVEILLANCE ACTIVITIES. 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. H1

    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. IF THE INFORMATION IS UNKNOWN, NOT AVAILABLE OR DOES NOT APPLY, THE SECTION/FIELD OF THE FORM IS LEFT BLANK. H10 ADDITIONAL NARRATIVE: D9: COMPLAINANT PART IS NOT EXPECTED TO BE RETURNED FOR MANUFACTURER REVIEW/INVESTIGATION. E3: REPORTER IS A J&J EMPLOYEE. H3, H6: THE INVESTIGATION COULD NOT BE COMPLETED; NO CONCLUSION COULD BE DRAWN, AS NO PRODUCT WAS RECEIVED. 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 (B)(6) 2022, THE PATIENT UNDERWENT SURGERY TO IMPLANT THE MINIBUNION IMPLANTS. ON (B)(6) 2023, THE OBLIQUE NON-LOCKING SCREW BACKED OUT POSTOPERATIVELY, REQUIRING A SURGERY TO REMOVE THE SCREW. BUNION CORRECTION WAS GOOD. THE IMPLANT HAD BEEN IN THE PATIENT FOR GREATER THAN 12 MONTHS. THIS REPORT INVOLVES ONE MINIBUNION, NON-LOCKING SCREW, 2.7MM X 14MM - STERILE. THIS IS REPORT 1 OF 1 FOR (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1618870 MINIBUNION NONLCKNG SCR 2.7MMX14MM STER PLATE, FIXATION, BONE HRS SYNTHES TRAUMA : CROSSROADS EXTREMITY SYSTEMS, LLC MINIBUNION, NON-LOCKING SCREW, 2.7MM X 14MM - STERILE 400290 00815432027019

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown Required Intervention