Events

Name: Generators for Spinal Cord Stimulation RM / Programmable Neurostimulator medtronic / Active Neurostimulator Technical Name: Implantable Pulse Generator for Neurostimulation Registration Number ANVISA: 10339190453 (model 97754) / 10339190310 (model 37754) / 10339190338 (model 37651) Class risk: IV 의 안전성 경고

Agência Nacional de Vigilância Sanitária (ANVISA)에 따르면, 해당 안전성 경고 는 Brazil 에서 MEDTRONIC COMERCIAL LTDA. 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
    2064
  • 날짜
    2016-10-17
  • 사례 국가
    Brazil
  • 사례 출처
    ANVISA
  • 사례 출처 URL
    http://www.anvisa.gov.br/sistec/alerta/consultaralerta.asp
  • 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
    #### UPDATED ON 7/24/2017, the company submitted the field action completion report verifying the sending of the customer safety notice. 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
  • 원인
    This field action is intended to provide important information about the noise response and beeper issue of the model 37751 chargers. this letter contains information on how to prevent this problem from occurring and how to restore the charger's operation if such an event occurs . the model 37751 chargers are sold as a kit with the model 37754 and 97754 charge systems for spinal cord stimulation (scs) and are also sold as a kit with the model 37651 charging system for deep brain stimulation (ecp).
  • 조치
    Field Action Code FA735 triggered under the responsibility of the company MEDTRONIC COMERCIAL LTDA. The company will make recommendations to health professionals.

Device

Name: Generators for Spinal Cord Stimulation RM / Programmable Neurostimulator medtronic / Active...

Manufacturer

MEDTRONIC COMERCIAL LTDA.
  • 제조사 모회사 (2017)
    Medtronic plc
  • 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