Covidien Devon Light Glove (included in multiple Procedure Packs) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Medline International Two 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-2017-RN-00064-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2017-01-13
  • 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 occasions, the devon light glove may split upon application to the devon light handle adapter. some of the reported splits resulted from difficult application of the light glove to the handle adapter. more recently, clinicians have reported finding splits in the light glove following surgery completion, where no difficulty in application of the light glove was encountered or finding splits directly out of the package. a split in the light glove causes a breach in the sterile field and can increase the potential for infection. there have been two reports in which splits were found at the conclusion of surgery.
  • 조치
    Medline is advising users to remove and discard the Covidien Light Glove from the procedure pack at the time of surgery preparation.

Device

  • 모델명 / 제조번호(시리얼번호)
    Covidien Devon Light Glove (included in multiple Procedure Packs)Multiple Product Codes ARTG Number for the Light Glove itself: 186761ARTG Numbers for the affected Procedure Packs containing the Light Glove: 140059, 136870, 137395, 140054 and 140058
  • Manufacturer

Manufacturer