Verso Shoulder Forked Retractor (Comprehensive Instrumentation (2 Prong Retractor)) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Biomet Australia 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-2016-RN-00206-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2016-02-24
  • 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
    An investigation has identified that verso shoulder forked retractor part number 402582 was manufactured using 420 stainless instead of 420 s29 stainless steel. 420 stainless steel is more brittle than 420 s29. the instrument may fracture during use. if the retractor fractures during surgery, surgical intervention may be necessary to retrieve any fractured pieces. a delay in surgery greater than 30 minutes may occur. if the pieces are unable to be retrieved, the patient would retain a foreign body.
  • 조치
    The sponsor is advising users to inspect stocks and quarantine the affected units. The sponsor will remove and replace the affected units. This action has been closed-out on 25/01/2017.

Device

  • 모델명 / 제조번호(시리얼번호)
    Verso Shoulder Forked Retractor (Comprehensive Instrumentation (2 Prong Retractor))Part number: 402852All Lots affectedARTG Number: 177811
  • 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