Spectra Optia Apheresis Systems 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Terumo BCT 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-2017-RN-00626-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2017-05-16
  • 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
    During routine testing by the manufacturer, a device that is similar to the spectra optia system demonstrated a non-recoverable power failure. a subsequent investigation determined that a power filter cable, a component used in the internal electrical system, had a visible defect that caused the unit to lose power. specific serial numbers of the spectra optia systems contain these cables and therefore there is a possibility these systems could encounter a non-recoverable power failure. if a power failure occurs prior to starting the procedure, the failure could result in the delay of the procedure until the device is repaired or another device is available. if a power failure occurs after the procedure has begun, the procedure cannot be completed, and automated rinseback cannot be performed.To date, the manufacturer has not received any customer reports of a non-recoverable power failure experienced in any spectra optia system with the possibly affected cables.
  • 조치
    Terumo is advising users that they will be replacing the affected cables. A Terumo sales representative will contact users to schedule a visit for the cable replacement. In the interim, the Spectra Optia system can continue to be used in accordance with the operator’s manual and the operator training materials, which include instructions for manual rinseback.

Device

  • 모델명 / 제조번호(시리얼번호)
    Spectra Optia Apheresis SystemsSerial Number Range: 1P04028 to 1P04392ARTG Number: 130529
  • Manufacturer

Manufacturer