BEUDAMED
    FDA Adverse Event Injury Summary report: N

    UNKNOWN PEEK INTERFERENCE SCREW

    MDR report key: 16121777 · Received January 9, 2023

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    Report

    Report Number
    1219602-2023-00045
    Event Type
    Injury
    Date Received
    January 9, 2023
    Report Date
    January 9, 2023
    Manufacturer
    SMITH & NEPHEW, INC.
    Product Code
    MAI
    PMA / PMN Number
    K142948
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NZ
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 0

    INTERNAL COMPLAINT REFERENCE: (B)(4). THIS COMPLAINT WAS OPENED BY SMITH+NEPHEW TO DOCUMENT A PATIENT COMPLICATION IDENTIFIED THROUGH A REVIEW OF THE NEW ZEALAND ACL REGISTRY AD HOC FROM NEW ZEALAND THAT INCLUDES REFERENCE TO THE USE OF A SMITH+NEPHEW PRODUCT. THE REPORTED ISSUE(S) RELATE TO KNOWN INHERENT PROCEDURAL RISKS THAT ARE APPROPRIATELY DOCUMENTED IN OUR RISK FILES. SMITH+NEPHEW WILL CONTINUE TO MONITOR TRENDS IN ACCORDANCE WITH OUR POST-MARKET SURVEILLANCE PROCESS AND TAKE NECESSARY ACTION AS REQUIRED IF ANTICIPATED SEVERITY AND/OR OCCURRENCE RATES ARE EXCEEDED. SMITH+NEPHEW HAS NO REASON TO SUSPECT THAT THE PRODUCT FAILED TO MEET ANY SPECIFICATIONS AT THE TIME OF MANUFACTURE. BASED ON OUR REVIEW OF ALL CURRENTLY AVAILABLE INFORMATION, WE ARE UNABLE TO CONFIRM A RELATIONSHIP BETWEEN THE REPORTED EVENT AND THE DEVICE OR IDENTIFY A DEFINITIVE ROOT CAUSE. HOWEVER, AS THE USE OF OUR PRODUCT CANNOT BE EXCLUDED AS A POTENTIAL CAUSE OR CONTRIBUTORY FACTOR TO THE REPORTED ISSUE, WE ARE CONSERVATIVELY SUBMITTING THIS REPORT IN ACCORDANCE WITH APPLICABLE REGULATIONS. IF ADDITIONAL INFORMATION BECOMES AVAILABLE THAT ALTERS THE CONCLUSIONS OF THIS REPORT, A FOLLOW-UP REPORT WILL BE SUBMITTED AS REQUIRED.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT ON REGISTRY REVIEW PMS-247 NEW ZEALAND ACL REGISTRY AD HOC REPORT FEB 2022 , 1 PATIENT PRESENTED A FAILED MENISCAL REPAIR AFTER AN ACL PROCEDURE USING A BIOSURE SCREW DEVICES. THE PATIENT REQUIRED AN ADDITIONAL SURGERY FOR MENISCAL REPAIR. PATIENT CURRENT STATUS IS UNKNOWN. NO FURTHER INFORMATION IS AVAILABLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2306217 UNKNOWN PEEK INTERFERENCE SCREW FASTENER, FIXATION, BIODEGRADABLE, SOFT TISSUE MAI SMITH & NEPHEW, INC. UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1 30 YR Female Required Intervention