RESTORESENSOR MULTI-PROGRAM RECHARGEABLE NEUROSTIMULATOR-CHARGING SYSTEM 의 리콜

Health Canada (via FOI)에 따르면, 해당 리콜 는 Canada 에서 MEDTRONIC OF CANADA 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
    49926
  • 사례 위험등급
    II
  • 사례 시작날짜
    2016-10-28
  • 사례 국가
  • 사례 출처
    HC
  • 비고 / 경고
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • 데이터 추가 비고
  • 원인
    Medtronic has identified an increased number of complaints from customers involving reports of rechargers that are in an unresponsive error state where the recharger is non-functional with a blank display screen and is beeping every 5 seconds. when this error state occurs the recharger is unable to recharge the neurostimulator until the recharger is reset. if the neurostimulator battery is allowed to become fully depleted this can lead to loss of therapy and return of associated diseasespecific symptoms. if the implanted neurostimulator battery is allowed to remain fully depleted it may overdischarge resulting in a permanent reduction in battery capacity and the need to recharge more frequently in the future. model 37751 ins rechargers that are used by patients to recharge their ins devices. notification will be provided to active implanting and managing physicians of both scs and dbs therapies. all model 37751 rechargers that are included in model 37651 37754 and 97754 kits may be affected by this issue. for a subset of patients receiving dbs therapy in rare instances a loss of dbs therapy may result in a life threatening injury or death. for example patients being treated for parkinson's disease may experience akinetic crisis and patients treated for epilepsy may experience status epilepticus. medtronic has not received any reports of life threatening injury or death associated with this issue.

Device

  • 모델명 / 제조번호(시리얼번호)
    Model Catalog: 37754 (Lot serial: All Lots); Model Catalog: 97754 (Lot serial: All Lots); Model Catalog: 37651 (Lot serial: All Lots)
  • 제품 설명
    RESTORESENSOR MULTI-PROGRAM RECHARGEABLE NEUROSTIMULATOR-CHARGING SYSTEM;CHARGING SYSTEM;ACTIVA RC NEUROSTIMULATOR - IMPLANTABLE NEUROSTIMULATOR RECHARGER
  • Manufacturer

Manufacturer

  • 제조사 주소
    BRAMPTON
  • 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
    HC