Events

Riata and Riata ST – all silicone coated models 를 위한 안전성 경고 / 현장 안전성 서한

Medicines and Healthcare products Regulatory Agency에 따르면, 해당 안전성 경고 / 현장 안전성 서한 는 United Kingdom 에서 St Jude Medical 에 의해 제조된 제품과 관련되어 있습니다.

이것은 무엇인가요?

현장 안전성 서한은 의료기기 제조사 또는 제조사 대리인이 시중에 유통되고 있는 자사 의료기기 제품에 대하여 취할 수 있는 조치를 알리는 소통방식입니다. 주요 대상층은 보건의료업계 종사자와 의료기기 사용자들입니다. 여기에는 회수(recall) 조치와 경고도 포함될 수 있습니다.

데이터에 대해 더 자세히 알아보기 여기
  • 사례 유형
    Safety alert / Field Safety Notice
  • 사례 ID
    MDA/2013/027
  • 사례 연번
    CON270680
  • 날짜
    2013-05-01
  • 사례 출판 날짜
    2013-05-01
  • 사례 국가
    United Kingdom
  • 사례 출처
    MHRA
  • 사례 출처 URL
    https://webarchive.nationalarchives.gov.uk/20150113054913/http://www.mhra.gov.uk/PrintPreview/MedicalDeviceAlertSP/CON270680?tabName=allTabs
  • 비고 / 경고
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • 데이터 추가 비고
  • 원인
    Improper use of peritoneal dialysis transfer sets may result in contamination, leading to infection or peritonitis. baxter healthcare ltd issued a field safety notice (fsn) in march 2013 to communicate various changes to the instructions for use (ifu).
  • 조치
    Identify affected devices. Ensure that all staff, who are responsible for placing and maintaining peritoneal dialysis transfer sets, are aware of the manufacturer’s FSN and the changes to the IFU. Ensure that all patients with these devices, who maintain their own transfer set, are aware of the patient advice in the FSN. This includes: the importance of maintaining aseptic technique. the appropriate use of chemical agents. that the use of excessive force can result in damage to the twist clamp. Return the customer reply form in the FSN to the manufacturer. The MHRA has previously issued advice on disinfecting and cleaning reusable medical devices with plastic surfaces to prevent damage.  See MDA/2013/019.

Device

Riata and Riata ST – all silicone coated models
  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Implantable cardioverter defibrillator (ICD) leads. Riata and Riata ST – all silicone coated models.
  • Manufacturer
    St Jude Medical

Manufacturer

St Jude Medical
  • 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
    MHRA