Terumo CDI Blood Parameter Monitoring System 500(Heart lung bypass in line blood gas monitor module) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Terumo 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-00487-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2016-04-28
  • 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
    The bpm sensor head assembly’s thermistor, which provides the blood temperature value does not meet specification. this may cause inaccurate temperature measurement and inaccurate analyte display values. the thermistor measurement takes longer to reach actual temperature and temperature measurements at the extremes (18°c and 37°c) are the most inaccurate. lowest temperature displayed was about 19°c for the thermistor when a different thermistor measured the temperature near 15°c. highest temperature displayed was about 32°c when a different thermistor measured about 37°c. inaccurate temperature measurement could also cause inaccurate measurements of other bpm values including potassium (k+), po2, pco2, and ph. the algorithms for these parameters rely on temperature for the calculations. inaccurate measurement of these values could result in inappropriate patient management. there have been no reports of injury.
  • 조치
    Terumo is advising users they can either; - Stop using the affected devices and return them to Terumo for repair. A loan unit will be provided until the corrected devices can be returned, OR - Continue to use the affected devices only for HSTAT monitoring functions until the replacement parts are available. These functions are unaffected by the issue. Once the replacement sensor heads are available, the devices should be returned to Terumo for repair. This action has been closed-out on 10/05/2017.

Device

  • 모델명 / 제조번호(시리얼번호)
    Terumo CDI Blood Parameter Monitoring System 500(Heart lung bypass in line blood gas monitor module)Catalogue numbers.: 500AHCT & 500AVHCTSerial numbers: 1899, 1948, 2473, 8001ARTG Number: 94012
  • 의료기기 분류등급
  • Manufacturer

Manufacturer