HomeChoice Pro Automated PD Cycler and HomeChoice Claria APD System 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Baxter Healthcare 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-00855-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2017-07-11
  • 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
    Baxter healthcare has been made aware that users may not be following the instructions in the operator’s manual and incorrectly opening disposable set packaging while setting up their peritoneal dialysis (pd) therapy, damaging the cassettes for the homechoice or homechoice pro cyclers. the homechoice cycler operator’s manual specifically warns the operator to open the disposable set packaging by hand and not use tools that may damage the cassette sheeting. do not use knives, scissors, clamp accessories, or other objects to open the disposable set packaging. if damaged cassettes are used, the cyclers may not consistently detect very small holes/cuts in the sheeting of the cassette in the patient valve region, and the cycler may deliver air into the patient.
  • 조치
    Baxter is requesting customers: 1. As stated in the At-Home Guide, open the packaging of the disposable set by hand. Do not use any sharp object to open the packaging; 2. Be aware that flow of fluid out of the connector at the end of the patient line after the prime phase of PD therapy is a visual indication of the potential for air delivery due to an undetected hole over the patient valve area in the cassette sheeting. Baxter will be updating the labelling to include this observation. 3. Complete the Customer Reply Form and return it as per the instructions in the customer letter; and 4. If you distribute this product to other facilities or departments within your institution, please forward a copy of this communication to them.

Device

  • 모델명 / 제조번호(시리얼번호)
    HomeChoice Pro Automated PD Cycler and HomeChoice Claria APD SystemHomeChoice PRO Automated PD Cycler, 230VProduct Code: R5C8320HomeChoice Claria APD System, 115V/230VProduct Code: 5C6M10All Serial NumbersARTG Number: 172780
  • Manufacturer

Manufacturer