Commercial Name: Revascularization Device Mindframe Capture LP. Technical Name: Clot Removal Device. ANVISA registration number: 10349000580. Risk class: IV. Affected model: 300010; 300011; 300012; 300013. Serial number affected: A568589; A560811; A544383 의 안전성 경고

Agência Nacional de Vigilância Sanitária (ANVISA)에 따르면, 해당 안전성 경고 는 Brazil 에서 Auto Suture do Brasil Ltda; Micro Therapeutics, Inc, d/b/a ev3 Neurovascular 에 의해 제조된 제품과 관련되어 있습니다.

이것은 무엇인가요?

안전성 경고는 의료기기 제품과 관련된 중요한 정보와 권고사항을 담고 있습니다. 물론 안전성 경고가 배포되었다고 해서 해당 제품이 무조건 안전하지 않은 제품이라는 것은 아닙니다. 보건의료업계 종사자와 의료기기 사용자들에게 배포되는 안전성 경고에는 회수(recall)도 포함될 수 있습니다. 제조사가 안전성 경고를 작성하기도 하지만, 보건당국에서 작성하는 경우도 있습니다.

데이터에 대해 더 자세히 알아보기 여기
  • 사례 유형
    Safety alert
  • 사례 ID
    2515
  • 날짜
    2018-03-12
  • 사례 국가
  • 사례 출처
    ANVISA
  • 사례 출처 URL
  • 비고 / 경고
    Brazilian data is current through June 2018. All of the data comes from Anvisa, 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 data from the U.S. and Brazil.
  • 데이터 추가 비고
    For the affected product that has not been used, Medtronic requests immediate action. 1. Remove and quarantine all unused products in your inventory. 2. Return the affected products to the Auto Suture (PLC). Your representative can help facilitate the return of the product as needed. 3. Complete the Customer Confirmation Form, and return it to the Auto Suture (PLC). If you wish to notify technical complaints and adverse events use the following channels: Notivisa: Notices of adverse events (AE) and technical complaints (QT) for products subject to Sanitary Surveillance should be made through the NOTIVISA System. To access the System, you must register and select the Health Professional option, if you are a liberal professional or the Institution / Entity option, if you are a professional of an institution / entity. Technovigilance System: Patient or citizen can notify through the Technovigilance System / SISTEC access through the link Additional information: - Date of identification of the problem by the company: 01/03/2018 - Date of notification notice for Anvisa: 08/03/2018 The company that owns the affected product is responsible for contacting its customers in due time. to ensure the effectiveness of the Field Action in progress. It stands out the joint responsibility of the distribution chain and use of health products in maintaining its quality, safety and efficacy, as well as the effectiveness of the Field Action, expressed by RDC 23/2012: "(...) Art 2 ° A holder of registration of health product is the holder of the registration / registration of health product with Anvisa. Single paragraph. The registration holder, as well as other agents involved from the production to the use of the product, or discarding it when applicable, are jointly and severally responsible for maintaining the quality, safety and efficacy of the health products to the final consumer. Art. 12 Distributors of health products shall forward to the registration holder, in a timely manner, the distribution map and other information requested for the notification and execution of field actions. (...) "
  • 원인
    Partial detachment or separation of the mindframe capture tm lp device may lead to vessel damage or the foreign body of the device may clog the bloodstream. potential complications or irreversible damage associated with this problem include, but are not limited to: prolonged procedure, incomplete treatment, internal damage, vasospasm, dissection, intracranial hemorrhagic, hematoma, transient ischemic attack, ischemic stroke / cerebral infarction, neurological deficit, and / or death. until february 23, 2018, auto suture (medtronic plc) has received a total of twenty (20) partial release or separation reports from the mindframe capturetm lp device. there were a total of three (3) reported serious damage reports, which include two (2) death reports potentially associated with this problem, we also report that these reports occurred outside brazil.
  • 조치
    Field Action Code FA804 triggered under the responsibility of the company Auto Suture do Brasil Ltda. It will make recollection.

Manufacturer

  • 제조사 모회사 (2017)
  • 제조사 의견
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Source
    ANVSANVISA