Devon Light Glove (Used as a cover with a compatible surgical light handle) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Covidien 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-01291-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2016-10-06
  • 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
    Customers have reported that on rare occasion (complaint rate less than 2/100,000 or 0.0017%), the devon light glove may split upon application to the devon light handle adapter. a subset of these splits reportedly resulted from a difficult application of the glove to the handle adapter. a split in the glove can potentially lead to a breach in the sterile barrier between the glove and the handle adapter. there have been no reports of serious injury associated with these rarely occurring splits.
  • 조치
    Medtronic is adding the statement "After application, inspect the Light Glove for barrier integrity" to the Devon Light Glove Instructions for Use (IFU) and notifying this information to the users through the customer letter.

Device

  • 모델명 / 제조번호(시리얼번호)
    Devon Light Glove (Used as a cover with a compatible surgical light handle)3611 Flexbl Lite Glove 1ea/pkgProduct Code: 311402083613 Lite GLV-Flexible 3ea/pkgProduct Code: 311402163612 Lite GLV-Flexible 2ea/pkgProduct Code: 31140257ARTG Number: 186761
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • 제조사 의견
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Source
    DHTGA