Rigid Arm Supports(used as part of Posiboard-2 and Positrest) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 alphaXRT 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-01031-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2017-08-09
  • 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 manufacturer civco radiotherapy have identified that specific units of rigid arm supports may have a height difference of approximately 17mm compared to those manufactured after july 2012.Due to the potential height variation in the rigid arm supports there is potential for mistreatment if there are multiple devices in the facility with varying heights between simulation and treatment. changes in arm position due to variation will impact the position of the chest wall and breast position. a 16.8mm variation in arm positioner could result in chest/breast/heart position changes which exceed expected treatment planning margins.
  • 조치
    alphaXRT is requesting Customers: 1. If your facility has an affected device and a newer device which is not included in the list, then usage should be immediately suspended; 2. Complete the supplied customer acknowledgment form and return it to NP@alphaXRT.com; 3. Retain a copy of the Customer Letter along with your most current product labelling; 4. Ensure relevant staff members are informed of this recall including relevant clinicians who may need to monitor for adverse events. 5. Place the notification letter in a prominent position for at least one month.

Device

  • 모델명 / 제조번호(시리얼번호)
    Rigid Arm Supports(used as part of Posiboard-2 and Positrest)Reference Numbers: 106047, 106015Lot Numbers: M164340, M178170, M165430, M165440, M191710 and M192470ARTG Number: 149575
  • 의료기기 분류등급
  • Manufacturer

Manufacturer