Events

MX 16-Slice CT scanner 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Philips Electronics Australia 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-2013-RN-00012-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2013-01-09
  • 사례 국가
    Australia
  • 사례 출처
    DHTGA
  • 사례 출처 URL
    https://apps.tga.gov.au/Prod/sara/arn-detail.aspx?k=RC-2013-RN-00012-1
  • 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
    Philips discovered that four screws that secure the patient table top to the carrier can become loose, causing the table top to detach.
  • 조치
    Phillips Healthcare is advising hospitals and radiology centres to inspect the patient table top screws. If the screws are not properly seated, discontinue use of the device and contact a Philips Field Service Engineer for repair. Philips Healthcare will contact their customers to schedule a time to replace the screws for all affected systems.

Device

MX 16-Slice CT scanner
  • 모델명 / 제조번호(시리얼번호)
    MX 16-Slice CT scannerSerial numbers: EP16E090006, EP16E110104, EP16E100082, EP16E120011, P16EM09002, EP16E100003ARTG Number: 158775
  • Manufacturer
    Philips Electronics Australia Ltd

Manufacturer

Philips Electronics Australia Ltd
  • 제조사 모회사 (2017)
    Philips
  • Source
    DHTGA