Device Recall Odyssey 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 PerMedics, Inc. 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
    55280
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-1609-2010
  • 사례 시작날짜
    2010-03-23
  • 사례 출판 날짜
    2010-05-18
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2012-07-30
  • 사례 출처
    USFDA
  • 사례 출처 URL
  • 비고 / 경고
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • 데이터 추가 비고
    system,planning,radiation therapy treatment - Product Code MUJ
  • 원인
    Anomaly 1, invalid characters in patient id error: currently, odyssey considers a valid id to be comprised of numbers and/or letters. if a patient id in a study contains a character other than a letter or number (including spaces). odyssey removes the invalid character when moving it to a patient folder. due to this, it is possible that two different patient studies could be listed within odyssey.
  • 조치
    A letter dated March 23, 2010 was mailed to customers acknowledging the anomalies and informed the reader that the mandatory version correcting the software will be provided by May 19, 2010. Customers with version 4.4 will receive 4.4.04:t hose with version 4.5 will receive 4.5.04; and those with version 4.6 will receive 4.6.01 containing the corrections to these issues. In the meantime, the following recommendations are provided. For Anomaly I . Invalid Characters in Patient ID Error, it 1s recommended that the users do not create patient IDS that contain characters other than letters or numbers. For Anomaly 2.0dysse.v Muchitle Library Collimator Type Error, it is recommended that the customer contact PerMedics ifany modifications to the library have been performed. The primary view should also be examined and used to detect and avoid the conditions causing the anomaly. Finally, independent field shape and monitor unit checks should be performed as part of a routine quality assurance program. For Anomaly 3, OOdyssey MLC Block Error, it is recommended to avoid using the MLC Block feature until the mandatory version correcting this anomaly is installed. If you need to use this feature, then it is recommended that a physical block tray is used during treatment for each beam that contains an Odyssey MLC Block. If customers believe a patient treatment has been affected by any of these issues, they should notify Customer Support as soon as possible at 877-4PerMed (877-473-7633) or support@permedics.com

Device

  • 모델명 / 제조번호(시리얼번호)
    Version 4.4 through 4.6
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Worldwide distribution: USA including NY, GA, CA, MA, and countries of Brazil, Hungary, China, India, Italy, Mexico.
  • 제품 설명
    Odyssey || Intended use: Radiation treatment planning system
  • Manufacturer

Manufacturer

  • 제조사 주소
    PerMedics, Inc., 1425 Victoria Ct, San Bernardino CA 92408-2853
  • 제조사 모회사 (2017)
  • Source
    USFDA