Uninterruptible Power Supply (UPS) for Philips CT / Advanced Molecular Imaging Systems 의 리콜

New Zealand Medicines and Medical Devices Safety Authority에 따르면, 해당 리콜 는 New Zealand 에서 Philips Medical Systems (USA) 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
    18335
  • 사례 시작날짜
    2015-04-09
  • 사례 국가
  • 사례 출처
    NZMMDSA
  • 사례 출처 URL
  • 비고 / 경고
    Data from New Zealand is current through July 2018. All of the data comes from the New Zealand Medicines and Medical Devices Safety Authority, 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 New Zealand.
  • 데이터 추가 비고
    Recalling Organisation: Philips New Zealand Commercial Limited, Level 3, 123 Carlton Gore Road, Newmarket, AUCKLAND 1023
  • 원인
    Philips has become aware of ups device failures that resulted in leaking of electrolyte (sulfuric acid), overheating and/or emission of fumes. analysis has identified that these failures are most likely due to batteries within the ups devices being held in service beyond their usable service life - typically three to five years.
  • 조치
    Manufacturer to issue advice regarding use

Device

  • 모델명 / 제조번호(시리얼번호)
    Model: BrightView X / XCT, Cardio MD, Forte, Gemini TF/ GXl (6 slice) / TF Astonish / 16 Power / GXL / TF 64 w/ TOF Performance, Precedence, Brilliance CT 16 Slice Air / 64 Channel / Big Bore / iCT / iCT - BETA TEST SYSTEM / iCT SP, Ingenuity CT / Core / Core128, Affected: All units
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    NZMMDSA