Image Archiving and Communication System (PACS), Model Syngo.Plaza; Registry 10234230177, Serial Numbers: 100193; 100180; 200284; 100220; 200298; 100222 and 100321 의 안전성 경고

Agência Nacional de Vigilância Sanitária (ANVISA)에 따르면, 해당 안전성 경고 는 Brazil 에서 Siemens Ltda.; SIEMENS AG 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
    1488
  • 날짜
    2014-12-22
  • 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
    The company informs that no case has been identified in Brazil. The record holder also informs that when an additional image is received, syngo.plaza may allocate the same file name to a new image, check that there is no file in the system, and after receiving the "available STS" signal, will add the entry of the new image in the database. Thus, there may be two references to the same image in the database. As soon as the new image is physically available on the STS, loading and archiving for both images will be indicated successfully, however, a mix of patient data may occur. - For the first series received, the incorrect image may be displayed, that is, for this series there may be an image with incorrect parameter, incorrectly scanned location such as head rather than knee and may have incorrect patient identification. This way, the text described in the image will not reflect the correct information. (The text described in the image will point to divergence of the patient name / area examined / analyzed parameter). - For the study received later, the image will be correct.
  • 원인
    Siemens identified a possible issue, which is currently being investigated and determined the need to verify syngo.Plaza with data file in status "2" (archived = true) for the sts short-term data storage, but not available in the long-term lts data storage. analyzes have shown that after restarting the process of receiving an image, a named and identified file can be used, which can cause a mixture of patient data. in this case, a subsequent acquisition operation of a new image may reuse the name of an already allocated image file. if this occurs, the system continues to operate and all subsequent operations will be processed successfully, however, a mix of patient data may have occurred. after you delete the affected file from the sts short-term data store, the inconsistency will be detected as other archiving failure operations.
  • 조치
    The company advises to wait for the Company's scheduling to update software and follow the guidelines contained in the letter, which should be archived. If you have any questions, please contact the Customer Service Center: 0800 55 48 38

Manufacturer