GYNEMESH PS and TVT DevicesGynemesh PS 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Johnson & Johnson Medical Pty Ltd 에 의해 제조된 제품과 관련되어 있습니다.

이것은 무엇인가요?

의료기기에 문제가 생겼을 경우 제조사가 이를 바로잡거나 시장에서 회수하는 조치를 말한다. 회수(Recall)는 의료기기에 결함이 있거나, 건강에 위협이 되거나, 또는 결함도 있고 건강에도 위협이 될 경우에 발생한다.

데이터에 대해 더 자세히 알아보기 여기
  • 사례 유형
    Recall
  • 사례 ID
    RC-2015-RN-00743-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2015-09-02
  • 사례 국가
  • 사례 출처
    DHTGA
  • 사례 출처 URL
  • 비고 / 경고
    Australian data is current through July 2018. All of the data comes from the Australian Therapeutic Goods Administration, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Australia.
  • 데이터 추가 비고
  • 원인
    Johnson & johnson medical pty. ltd. (jjm) is issuing a notification to inform hospitals and surgeons of changes to the instructions for use (ifu) for ethicon gynemesh ps and tvt devices.The changes include additional information on adverse reactions, warnings, precautions and patient selection.
  • 조치
    Johnson & Johnson Medical (JJM) is issuing a notification to inform hospitals and healthcare professionals of changes to the Instructions for Use (IFU) for Ethicon GYNEMESH PS and TVT Devices. These changes have been made following the TGA’s clinical review of urogynaecological meshes and include additional information on include additional information on adverse events, warnings and contra-indications. This action has been closed-out on 22/08/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    GYNEMESH PS and TVT DevicesGynemesh PSProduct Codes: GPSL and GPSXL3; TVT DevicesProduct Codes: 810041A, 810041B, 810081, TVTRL, TVTOML ARTG Number: 99193 (TVT) & 165075 (Gynemesh PS)
  • Manufacturer

Manufacturer