Patient Data Module (PDM) Used with CARESCAPE Monitor B850, B650, or B450 (Multiparameter Patient Monitor) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 GE Healthcare 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-2014-RN-00945-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2014-08-29
  • 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
    Ge healthcare has recently become aware of a potential safety issue due to ecg performance issues following a disconnect/reconnect cycle with the patient data module (pdm), when used with the carescape bx50 monitors. if the pdm is quickly disconnected and reconnected (less than 10 second cycle) from a carescape bx50 monitor following a “patient discharge” or during active monitoring, the ecg waveform and its associated waveform parameters could be analysed incorrectly and the alarms for serious conditions may not be triggered appropriately. the ecg heart rate (hr) parameter data, the ecg waveform analysis and other ecg parameter measurements are displayed at values that will be less than the actual patient's physiologic condition. the issue potentially affects heart rate, ecg st segment analysis, 12 lead ecg analysis; ecg, spo2, respiration and invasive blood pressure waveforms both locally and at cic; and data displayed at cic may show data drop out.
  • 조치
    To prevent the occurrence of the issues, when physically disconnecting the PDM from the CARESCAPETM Monitor Bx50 users should wait a minimum of 10 seconds before reconnecting. If users notice the ECG heart rate value appears to be half of the patient's physiologic condition or the patient waveforms (ECG, SpO2, Invasive Blood Pressure, or Impedance Respiration) appear to show every other pulse, follow these steps to correct the parameter and alarm issues: 1)Physically disconnect the PDM E-port cable or un-dock the PDM from the host monitor. 2)Wait a minimum of 10 seconds and then reconnect or re-dock the PDM. When the PDM re-establishes communication with the Bx50, the parameters and alarms will operate as expected. GE Healthcare will also implement a permanent software fix.This action has been closed-out on 15/08/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    Patient Data Module (PDM) Used with CARESCAPE Monitor B850, B650, or B450 (Multiparameter Patient Monitor)All versions of PDM software v2.2 or lowerARTG number: 92726
  • Manufacturer

Manufacturer