Mako Internal cPCI Card Cage 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Stryker 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-00857-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2017-07-11
  • 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
    Stryker has determined that during assembly of the cpci card cage, a potential cross threading of the 3.3 vdc lug may exist. visual inspection did not confirm the assembly error. this condition could result in an intermittent power connection in the cpci card cage and abnormal system behaviour or a total loss of power. powering down of the system due to intermittent or total loss of power is estimated to have a probability of occurrence at 0.0022%. this would make the system temporarily unavailable. potential harms resulting in this failure mode are extended surgical time of =15 minutes or extended surgical time of >30 minutes.
  • 조치
    Stryker is requesting customers: 1. Inform users of this Recall for Product Correction and forward the notice supplied to all internal staff who need to be aware of this issue; 2. A Stryker representative will coordinate a time for the inspection and, if necessary, replace the cPCI Unit. The Mako may continue to be used in the meantime; 3. Complete the supplied “Recall for Product Correction Notification Response” form to acknowledge you have seen this letter. Return the completed form to Stryker by email to recalls@stryker.com or fax on (02) 9467 1325; and 4. If affected stock could have been transferred from your hospital to another location, please immediately let them know of this recall action.

Device

  • 모델명 / 제조번호(시리얼번호)
    Mako Internal cPCI Card CageItem Number: 201337Lot Number: 05212015ARTG Number: 223105
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    DHTGA