Events

Device Recall Nuclear Magnetic Resonance Imaging System 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 GE Medical Systems, LLC 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
    51314
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-1723-2009
  • 사례 시작날짜
    2008-11-03
  • 사례 출판 날짜
    2009-08-25
  • 사례 상황
    Terminated
  • 사례 국가
    United States
  • 사례 종료 날짜
    2012-05-24
  • 사례 출처
    USFDA
  • 사례 출처 URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=80290
  • 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, nuclear magnetic resonance imaging - Product Code LNH
  • 원인
    Ge healthcare has identified a potential pinch point hazard on ovation mr scanner when using ctl array xl body flex and opened body coil. a patient's hand may be pinched between the magnet bore ceiling cover and the ctl array, xl body flex, or open body coil if the patient puts his/her hand on the top of the coil. two injuries and four complaints filed. 2/20/09: recall being expanded to incl.
  • 조치
    GE Healthcare issued a "Product Safety Notification" letter dated October 23, 2008. The letter was addressed to Hospital Administrators, Mangers of Radiology/Cardiology & Radiologists/Cardiologists. The letter described the Safety Issue, Affected Product, Safety Instructions, Product Correction and Contact Information for the Signa Ovation 0.35T Systems. A second GE Healthcare "Urgent Medical Device Correction" letter dated March 5, 2009 was sent 3/9/09 to consignees which addressed the expanded recall to the Signa OpenSpeed0.7T MR Systems. For further questions, contact your local GE Healthcare sales or service representative.

Device

Device Recall Nuclear Magnetic Resonance Imaging System
  • 모델명 / 제조번호(시리얼번호)
    Model Number: 2138300-30;  Serial Numbers: 00000203387MR6, 00000208208MR9, 00000216409MR3, 00000229302MR5, 00000229306MR6, 00000230309MR7, 00000231588MR5, 00000237930MR3, 00000239847MR7, 00000241694MR9, 00000247255MR3, 00000253103MR6, 00000189633MR1, 00000192104MR8, 00000193652MR5, 00000194218MR4, 00000194219MR2, 00000194950MR2, 00000196364MR4, 00000197334MR6, 00000198709MR8, 00000199443MR3, 00000201708MR5, 00000201709MR3, 00000201710MR1, 00000201901MR6, 00000202223MR4, 00000203386MR8, 00000204837MR9, 00000204838MR7, 00000204839MR5, 00000206438MR4, 00000206439MR2, 00000207493MR8, 00000207494MR6, 00000208209MR7, 00000208210MR5, 00000209712MR9, 00000209713MR7, 00000212511MR0, 00000212513MR6, 00000212514MR4, 00000212515MR1, 00000215366MR6, 00000216405MR1, 00000216406MR9, 00000216407MR7, 00000216409MR3, 00000217198MR1, 00000217201MR3, 00000221250MR4, 00000221251MR2, 00000221253MR8, 00000221254MR6, 00000222950MR8, 00000225273MR2, 00000225274MR0, 00000225942MR2, 00000226318MR4, 00000228022MR0, 00000228023MR8, 00000228024MR6, 00000228773MR8, 00000229303MR3, 00000229304MR1, 00000229305MR8, 00000230308MR9, 00000230312MR1, 00000231591MR9, 00000231592MR7, 00000232328MR5, 00000233644MR4, 00000233646MR9, 00000234832MR4, 00000234833MR2, 00000234834MR0, 00000237051MR8, 00000237052MR6, 00000237053MR4, 00000237926MR1, 00000237927MR9, 00000237928MR7, 00000237929MR5, 00000239480MR7, 00000239482MR3, 00000239483MR1, 00000239484MR9, 00000239845MR1, 00000239846MR9, 00000241126MR2, 00000241127MR0, 00000241693MR1, 00000241695MR6, 00000243405MR8, 00000244231MR7, 00000244232MR5, 00000247252MR0, 00000247253MR8, 00000247254MR6, 00000247256MR1, 00000250184MR9, 00000250185MR6, 00000250186MR4, 00000250187MR2, 00000253039MR2, 00000253102MR8, Unknown;  Model Number: 2377062-5;  Serial Numbers: 00000000100YR8, 00000000119YR8, 00000000129YR7, 00000000102YR4, 00000000103YR2, 00000000105YR7, 00000000106YR5, 00000000108YR1, 00000000109YR9, 00000000111YR5, 00000000113YR1, 00000000118YR0, 00000000120YR6, 00000000122YR2, 00000000124YR8, 00000000127YR1, 00000000128YR9, 00000000131YR3, 00000000132YR1, 00000000133YR9, 00000000134YR7, 00000000135YR4, 00000000136YR2, 00000000137YR0, 00000000142YR0, 00000000144YR6, 00000000146YR1, 00000000149YR5, 00000000150YR3, 00000000151YR1, 00000000152YR9, 00000000155YR2, 00000943610YM6, 00000951021YM5, 00000962592YM2;  Model Number: 2377062-30  Serial Numbers: 00000003047YR8, 00000003011YR4, 00000003022YR1, 00000003023YR9, 00000003024YR7, 00000003025YR4, 00000003026YR2, 00000003027YR0, 00000003028YR8, 00000003029YR6, 00000003030YR4, 00000003031YR2, 00000003033YR8, 00000003034YR6, 00000003035YR3, 00000003036YR1, 00000003039YR5, 00000003041YR1, 00000003042YR9, 00000003043YR7 and 00000003044YR5.
  • 의료기기 분류등급
    Radiology Devices
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Worldwide Distribution-- US (including states of AL, ALZ, AR, CA, CO,CT, DE, FL, FA, IL, IN, IA, KS, KY, LA, MD, MA, MI, MN, MS, MT, MO, NE,NH, NV, NJ, NY, NC, OH, OK, OR, PA, PR, SC SD, TN, TX, VA, WA, WV and WI), CHINA, CYPRUS, ARGENTINA, BRAZIL EGYPT, DENMARK, FEDERAL REPUBLIC OF GERMANY, FEDERAL REPUBLIC OF FRANCE, GET 7 D CHINA, GREECE, HUNGARY, ITALY, IVORY COAST, JAPAN, KOREA, KUWAIT, MALAWI, MEXICO, OMAN, PANAMA, PHILIPPINES, RUSSIAN FEDERATION, SAUDI ARABIA, SPAIN , SWITZERLAND, TURKEY, UKRAINE, UNITED ARAB EMERITUS, UNITED KINGDOM and VENEZUELA.
  • 제품 설명
    Signa Openspeed 0.7T MR Systems, Model Numbers: || Openspeed 3 (2138300-30), Openspeed 4 (2377062-5), Openspeed 5 (2377062-5, 2377062-30)
  • Manufacturer
    GE Medical Systems, LLC

Manufacturer

GE Medical Systems, LLC
  • 제조사 주소
    GE Medical Systems, LLC, 3000 N Grandview Blvd, Waukesha WI 53188-1615
  • 제조사 모회사 (2017)
    General Electric Company
  • Source
    USFDA