Events

Device Recall GE Innova 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Datex - Ohmeda, 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
    49538
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-1522-2008
  • 사례 시작날짜
    2008-05-19
  • 사례 출판 날짜
    2008-09-30
  • 사례 상황
    Terminated
  • 사례 국가
    United States
  • 사례 종료 날짜
    2016-06-30
  • 사례 출처
    USFDA
  • 사례 출처 URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=73765
  • 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
    Solid State X-Ray Imager - Product Code MQB
  • 원인
    Ge healthcare has become aware of a potential condition that may impact operator or patient safety. one customer has reported that inability to terminate x-ray exposure after releasing the hand switch control (located in the control room).
  • 조치
    An Urgent Medical Device Correction letter, dated June 2008 was sent to customers The letter described the issue, affected products and provided short term user recommendations. GE developed a new software release that corrects this condition and will launch the corrective action to upgrade all affected systems.

Device

Device Recall GE Innova
  • 모델명 / 제조번호(시리얼번호)
    Systems id: 77573841, 80158241, 910063039, 3018774100, 4103374100, 4438494100, 5134754100, 5138534100, 6029234100, 8159374100, 8595724100, 9408984100, 82406010011, 082416130011, 82416130012, 00095VAS07, 205759CL2, 216844INNOVA, 229228INNOV41V, 229434INNOV, 239436CATH1, 251435ICV5, 304255INNOVA, 304347INNOVA, 315448RM4, 315448RM5, 319338VA4100, 325670CATH, 337981INNOVA, 352333VASC, 352376SP, 352401CATH, 352401VASC, 407518SP2, 407518SP3, 407SPECIALS, 414961INN4100, 478633INOV, 508856OR41, 515263IL4100, 516562INNOVA4, 573632CRA, 573761SMA, 574535IN41, 600050VA01, 6012884100SP1, 606833INNOVA, 609652CATH3, 614293LIBERTY1, 614293LIBERTY2, 704487CR41, 706802FINN, 715369INN4100, 717763INNOVA41, 717763OR4100, 718518CVL1, 724656ANG, 727725SPEC1, 727819SPSC, 740592INNOVA, 757398INNOVA, 757736INNOVA, 803329CL41, 804320CATH2B, 804594CATH, 812279INNOVA1, 813972INTV, 816276SP1, 817255NH4100, 828696IN41, 865541CCL5, 865693CCL3, 901726SP2, 903CSM4100, 904276SP, 906485ANGIO, 918307SHIN4, 941483INNOVA41, 956632INN4100, A5630803, B5801711, BE5005VA01, BY4020VA01, RU1018VA03, SA1188VA03, SLIN4100, YV0003.
  • 의료기기 분류등급
    Radiology Devices
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Worldwide Distribution - AL, AZ, CA, FL,, GA, HI, IA,IL, IN, KY, LA,MA, MD, MI, MO, MS, NC, NH, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WI, and WV, Puerto Rico. OUS to include: Australia, Byelarus, China, Denmark, France, Germany, Greece, Honduras, Iran, Iraq, Italy, Japan, Latvia, Lebanon, Mexico, Poland, Russia, Saudi Arabia, Turkey, United Kingdom, and Venezuela.
  • 제품 설명
    GE Healthcare Innova 4100 Digital Fluoroscopic Imaging (Cardiovascular Imaging System
  • Manufacturer
    Datex - Ohmeda, Inc

Manufacturer

Datex - Ohmeda, Inc
  • 제조사 주소
    Datex - Ohmeda, Inc, Po Box 7550, Madison WI 53707
  • Source
    USFDA