4F Stiffened Micro-Introducer Kits (guidewire or catheter introducer) Product Description: STF 4F M.I. KIT 45CM NT/T ECHO S PG 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Medical Specialties 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-2016-RN-01295-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2016-10-11
  • 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
    Angiodynamics, inc., the manufacturer of the 4f stiffened micro-introducer kits, has become aware of the potential with respect to the 4f sheath/dilator components for the rotating luer to detach from the dilator hub during use.Use of the affected angiodynamics stiffened micro-introducer kits may result in patient harm, including minor tissue trauma and/or minor delay in procedure to replace the device.
  • 조치
    Medical Specialties Australia have contacted affected customers and retrieved all unused product. This action has been closed-out on 24/05/2017.

Device

  • 모델명 / 제조번호(시리얼번호)
    4F Stiffened Micro-Introducer Kits (guidewire or catheter introducer)Product Description: STF 4F M.I. KIT 45CM NT/T ECHO S PGCatalogue Number: 06597052Lot Numbers: 5031722 & 5043440ARTG Number: 172522
  • Manufacturer

Manufacturer