All models and lot numbers of silicone gel filled breast implants 를 위한 안전성 경고 / 현장 안전성 서한

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

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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 연번
    MDA/2010/025
  • 날짜
    2010-03-31
  • 사례 출판 날짜
    2014-12-17
  • 사례 국가
  • 사례 출처
    MHRA
  • 사례 출처 URL
  • 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
    On Tuesday 30 March 2010 the French medical device regulatory authority (AFSSAPS) informed the MHRA that it has suspended the marketing, distribution, export and the use of silicone gel filled breast implants manufactured by PIP (a French breast implant manufacturer). It has recalled all of these devices.AFSSAPS recently carried out an inspection of the PIP manufacturing plant and established that most breast implants manufactured by the company since 2001 have been filled with a silicone gel with a composition different from that approved.The MHRA does not yet know if the use of the unapproved material affects the safety of the implants. We understand that AFSSAPS is carrying out urgent testing and has undertaken to provide further information as soon as it is available.The MHRA will provide further advice on patient management, as necessary, when more information is available.
  • 원인
    (poly implant prothese (pip)) french medical device regulatory authority (afssaps) found the composition of silicone gel for most breast implants have been different to the one approved since 2001 (mda/2010/025).
  • 조치
    Implanting centresDo not implant these devices Quarantine and return all of these devices to the distributorGPsAdvise patients who are concerned about their PIP implants to consult their implanting surgeon.Implanting surgeonsAwait further advice from the MHRA regarding clinical management of patients implanted with these devices.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Silicone gel filled breast implants manufactured by Poly Implant Prothese (PIP). All models and lot numbers.
  • Manufacturer

Manufacturer

  • 제조사 주소
    Andrew Hay (Director) Clover Leaf Products Ltd 6-10 Church Farm Courtyard High Street Chalfont St Giles HP9 4QH Tel: 01494 876 990 Fax: 01494 876 991Email: andy@cloverleafproducts.com(company name corrected August 2010)
  • 제조사 모회사 (2017)
  • Source
    MHRA