Events

Riata and Riata ST Silicone Endocardial Defibrillation Leads 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 St Jude Medical 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-2013-RN-00692-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2013-07-05
  • 사례 국가
    Australia
  • 사례 출처
    DHTGA
  • 사례 출처 URL
    https://apps.tga.gov.au/Prod/sara/arn-detail.aspx?k=RC-2013-RN-00692-1
  • 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
    This is an update to the 'hazard alert' letter in may 2012 and subsequent update in july 2012 (tga ref.: rc-2012-rn-00391-3) and highlights the following topics: (1) key studies and patient management considerations for patients with riata and riata st silicone leads; (2) the most recent riata lead evaluation study results; and (3) the 2013 1st edition product performance report (ppr).The may 2012 'hazard alert' identified that externalised conductors can occur in riata and riata st silicone leads when an abrasion results in an outer insulation breach within the vascular or cardiac systems allowing the normally contained conductors to become visible outside the lead body. externalised conductors can be a result of relative motion of the conductor cables within the lead insulation lumen, referred to as inside-out abrasion, or from external sources of abrasion, e.G. lead-to-lead abrasion, where the outer insulation is breached.
  • 조치
    St Jude Medical is providing updated clinical information to treating clinicians based on the interim results from the ongoing studies on the performance of the Riata and Riata ST leads in long term clinical use related to insulation wear and lead conductor externalisation. Detailed data has been provided by the manufacturer at www.riatacommunication.com

Device

Riata and Riata ST Silicone Endocardial Defibrillation Leads
  • 모델명 / 제조번호(시리얼번호)
    Riata and Riata ST Silicone Endocardial Defibrillation LeadsRiata (8Fr): Models 1560, 1561, 1562, 1570, 1571, 1572, 1580, 1581, 1582, 1590, 1591, 1592Riata ST (7Fr): Models 7000, 7001, 7002, 7010, 7011, 7040, 7041, 7042All these models have been cancelled from the ARTG
  • 의료기기 분류등급
    Cardiovascular Devices
  • Manufacturer
    St Jude Medical Australia Pty Ltd

Manufacturer

St Jude Medical Australia Pty Ltd
  • 제조사 모회사 (2017)
    Abbott Laboratories
  • 제조사 의견
    “We are in constant communication with regulatory agencies and competent authorities worldwide which allows us to implement global recalls or in-country communication quickly and effectively,” Abbott, which now owns St. Jude Medical told ICIJ in a statement. In addition to sending global notices to physicians worldwide, we also make sure that product advisories are available online and classification of product recalls and product advisories are determined by global regulatory bodies which can impact the timing in any given country. MD companies follow varying regulations in different countries. In come countries software is not regulated so a recall in one country related to software would not be classified as a recall or field action in another. In addition, review cycles within the regulatory process can be different in each country which can impact communication and recall timing.
  • Source
    DHTGA