UNIVERSAL Modular Electric/Battery Double Trigger Handpiece (Surgical power tool) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Zimmer 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-2014-RN-01068-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2014-10-17
  • 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
    Zimmer surgical identified a potential malfunction on the universal modular electric/battery double trigger handpiece. it is possible that the handpiece could start by itself when the power source is connected. the unexpected output of the device (start by itself) could lead to an injury to the user during usage or preparation of the device. the complaint rate for this occurrence is 0.5% per distributed device, and no injuries have been reported.
  • 조치
    To avoid this potential issue (malfunction), Zimmer Surgical is advising customers to implement temporary workaround instructions through the customer letter. Zimmer Surgical, as part of the annual preventive maintenance activities, will upgrade the devices with the new electronics that prevent the “self-start” issue and may also exchange other components as appropriate during the preventive maintenance check. This action has been closed-out on 06/06/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    UNIVERSAL Modular Electric/Battery Double Trigger Handpiece (Surgical power tool)Model number: 89-8507-400-00ARTG Number 215808
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • 제조사 의견
    “The safety of patients has always been, and continues to be, Zimmer Biomet’s top priority and it is our honor to be a leader in this industry for the past 90 years,” Zimmer Biomet told ICIJ in a statement. “We adhere to strict regulatory standards, and work closely with the FDA and all applicable regulatory agencies in each of our regions as part of our commitment to operating a first-rate quality management system across our global manufacturing network. The company added that it is focused on staying at the forefront of innovation and doing right by the millions of patients who rely on the company’s products.
  • Source
    DHTGA