Manual Collimator Exchange system in use with an ADAC VERTEX Plus, CARDIO, SOLUS or VERTEX V60 imaging system(Nuclear Medicine Gamma Camera Systems) 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-2015-RN-00400-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2015-05-15
  • 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
    Philips healthcare received a report that during a manual collimator exchange procedure, when the operator was attempting to slide the collimator cassette from the collimator storage cabinet onto the collimator exchange carriage, the cassette did not align with the carriage top guide rollers and mechanical lock. the collimator and collimator cassette fell off the carriage resulting in the operator receiving a minor injury. this could result in serious injury to a person if it comes in direct contact with the operator. automatic collimator exchange system is not affected.
  • 조치
    Philips Healthcare is instructing their customer not to proceed with collimator exchange procedure, if a misalignment on the top and/or bottom of the guide rail between the cabinet and carriage can be visually detected Philips Healthcare service technician will fix the issue prior to the continued use of the system. UPDATE: Philips is advising their customer that they must ensure collimator alignment is inspected via regularly scheduled Preventive Maintenance at 3 month intervals. An updated procedure for inspecting collimator alignment has been provided. This action has been closed-out on 10/08/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    Manual Collimator Exchange system in use with an ADAC VERTEX Plus, CARDIO, SOLUS or VERTEX V60 imaging system(Nuclear Medicine Gamma Camera Systems)ARTG number: 117642
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    DHTGA