A5 ANESTHESIA DELIVERY SYSTEM 의 리콜

Health Canada (via FOI)에 따르면, 해당 리콜 는 Canada 에서 SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO. 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
    19731
  • 사례 위험등급
    III
  • 사례 시작날짜
    2017-07-17
  • 사례 국가
  • 사례 출처
    HC
  • 비고 / 경고
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • 데이터 추가 비고
  • 원인
    Mindray has become aware of the potential for a software anomaly to manifest on the a-series anesthesia system. no adverse patient event was reported. this potential issue is related to the system's electrically erasable programmable read-only memory (eeprom) and will only occur if the system's total number of write cycles to a particular range of memory locations has exceeded the life specification of the eeprom. the issue will only manifest at start up or at the end of a case.It will not occur during a case.Two scenarios may occur resulting from this issue.1) the unit will not be able to enter standby mode when the user confirms "discharge" (in software bundle version < 02.06.00) or "end case" (in software bundle version > 02.06.00) in the dialog box. under these conditions the unit can only enter the standby mode by manually unchecking "restore default settings" in the same dialog box.When the "restore default settings" in the dialog box is unchecked the previous settings will be applied to the next case instead of the user established default settings.If left unaddressed for a period of time this second scenario will be encountered.2) at startup the unit will automatically skip over the startup leak test as well as standby mode and immediately enter either manual or automatic ventilation mode depending on the position of the manual/auto switch.This potential issue affects a-series systems with software bundle version 02.02.00 through 02.11.00 and some units with 02.11.01.

Device

  • 모델명 / 제조번호(시리얼번호)
    Model Catalog: 0631B-PA00012 (Lot serial: 0.02.00-02.11.00 SOFTWARE); Model Catalog: 0632B-PA00014 (Lot serial: )
  • 제품 설명
    A-Series (A5/A7) Anesthesia Delivery System
  • Manufacturer

Manufacturer