MEDPOR Facial and Oculoplastic Sizer Sets and TLS Drain System 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-00052-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2017-01-11
  • 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
    A report has been received indicating that the outer label of a medpor sizer set states ‘sterile’, whereas the product is actually delivered non-sterile. investigations have revealed that additional products and lots have an incorrect sterility status on their labels. the introduction of a non-sterile device into the sterile surgery field could potentially cause infection requiring additional medical or surgical treatment.
  • 조치
    Stryker is advising users to inspect their inventory and quarantine affected stock. They are requested to contact Stryker to coordinate the return of affected products for a resupply or a credit. This action has been closed out on 16 June 2017.

Device

  • 모델명 / 제조번호(시리얼번호)
    MEDPOR Facial and Oculoplastic Sizer Sets and TLS Drain SystemItem Numbers: 6630, 9951, 9952Multiple Lot NumbersARTG Numbers: 258033, 264273
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    DHTGA