Atrium Chest DrainsOcean Drains 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Maquet 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-01580-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2016-12-06
  • 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
    Atrium chest drainage products are packaged with a double sequential sterile wrap and placed into an outer dust cover. the dust cover is folded over and secured with the package label. the label on the outer package denotes the product as being sterile. the chest drain inside the packaging is sterile; the outer dust cover is not sterile. the two sterilisation wraps are what provide the sterile barrier for the product. this packaging system is the same configuration used on atrium chest drainage products for the past 30 years. maquet is providing users with clarification as to which part of the packaged drain is sterile. in addition, maquet is advising that product manufactured after october 18 2016 will contain a new warning label that identifies the pouch as not being a sterile barrier and warns the user that only the chest drain can be entered into the sterile field.
  • 조치
    Maquet is informing users of the following steps for introduction of the Atrium Chest Drains into the sterile field; To introduce the chest drain into the sterile field: 1. Remove the wrapped chest drain from the dust cover. 2. Open the 2 sterilisation wraps using sterile technique. 3. Only enter the chest drain into the sterile field. Maquet is also providing the new warning label that product manufactured from October 18 2016 will contain, and is requesting users to post copies of this label near all Atrium chest drain product inventory with expiration date prior to October 2019. This action has been closed-out on 26/05/2017.

Device

  • 모델명 / 제조번호(시리얼번호)
    Atrium Chest DrainsOcean DrainsModel Numbers: 2002-300, 2012-320, 2050-300Oasis DrainsModel Numbers: 3600-100, 3612-100, 3612-100, 3620-100Express DrainsModel Numbers: 4000-100N, 40120-100NExpress MiniModel Number: 16400All Lot Numbers with Expiration Date Prior to October 2019ARTG Number: 119726
  • Manufacturer

Manufacturer