Cheek Retractor, f/MatrixMANDIBLE U-shaped, flexible 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Synthes 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-01366-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2014-12-24
  • 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 cheek retractor for matrixmandible u-shaped may not function as intended due to the potential for corrosion and/or failure of the internal spring which has been manufactured from an incorrect material. as an internal part of the instrument, the spring is not in direct contact with the patient. however, in the event that the spring or a subcomponent of the spring was to fail and/or corrode, the possibility exists that the particles may transfer from the instrument to the patient, potentially leading to an adverse tissue reaction and/or infection. a surgical delay may also arise if the retractor does not work during a procedure and a replacement needs to be found.To date, there have been no reports of adverse events related to this issue.
  • 조치
    Customers are asked to inspect invetory and to follow the instructions provided for any affected units. To mitigate risk, should customers with affected instruments require the instrument for emergency cases, please perform a visual and functional inspection, as detailed in the cistomer letter, prior to, during and after use. Customers are asked to exercise caution regarding the risk of corrosion or spring breaking during the procedure. This action has been closed-out on 04/04/2017.

Device

  • 모델명 / 제조번호(시리얼번호)
    Cheek Retractor, f/MatrixMANDIBLE U-shaped, flexiblePart Number: 397.232Multiple lot numbers affectedARTG Number: 153950
  • Manufacturer

Manufacturer