Events

Rappel de GE Healthcare Infinia Hawkeye 4

Selon U.S. Food and Drug Administration, ce/cet/cette rappel concerne un dispositif en/au/aux/à United States qui a été fabriqué par GE Medical Systems, LLC.

Qu'est-ce que c'est?

Une correction ou un retrait opéré par un fabricant afin de répondre à un problème causé par un dispositif médical. Les rappels surviennent lorsqu'un dispositif médical est défectueux, lorsqu'il pourrait poser un risque pour la santé, ou les deux à la fois.

En savoir plus sur les données ici
  • Type d'événement
    Recall
  • ID de l'événement
    50990
  • Classe de risque de l'événement
    Class 2
  • Numéro de l'événement
    Z-1095-2009
  • Date de mise en oeuvre de l'événement
    2008-09-08
  • Date de publication de l'événement
    2009-04-10
  • Statut de l'événement
    Terminated
  • Pays de l'événement
    United States
  • Date de fin de l'événement
    2012-05-24
  • Source de l'événement
    USFDA
  • URL de la source de l'événement
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=78029
  • Notes / Alertes
    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.
  • Notes supplémentaires dans les données
    Emission computed tomography system - Product Code KPS
  • Cause
    There is a possibility for misregistration when brain scans are performed with infinia with the hawkeye option. this misregistration could present the potential for misdiagnosis when the patient headrest sags under the weight of a head.
  • Action
    Consignees were sent from September 2008 - Feb 2009 a GE "Product Safety Notification" letter dated 4/2008. The letter was addressed to Hospital Administrators, and Managers of Radiology/Cardiology, Radiologists/Cardiologists. The letter described the Safety Issue, Affected Product, Safety Instructions, Product Correction and Contact Information. It instructed consignees to continue to use the Infinia Hawkeye system normally for all types of Hybrid scans and stated that as a general practice tomograms should be reviewed carefully using the Xeleris Volumetrix processing protocol to ensure proper registration. Local sales or service reps should be contacted for further information regarding the notification.

Device

GE Healthcare Infinia Hawkeye 4
  • Modèle / numéro de série
    H3000WC : S/N 17032 17391 16844 17215 16974 16979 17090 16898 16967 17136 17057 17130 17121 17337 17298 17376 17208 17114 16876 17164 17247 17276 17286 17293 17317 17070 17391 17220 16905 17011 16850 16947 17347 17082 16880 16910 17288 16933 17061 17198 16994 17265 16820 17106 17058 17047 17053 17116 16852 17169 17169 17029 17195 17169 16938 17125 16970 16774 17226 16886 17118 16945 17348 16924 16888 16811 17122 17389 17020 17135 16962 17101 16849 17233 17137 17300 17299 17268 16960 17326 17050 17269 17131 17204 17349 17034 17005 17213 17301 17019 16987 17108 17088 17166 17287 17099 17023 16927 17328 17174 17042 16821 16914 16972 17285 17323 17104 17241 17258 17249 17109 16977 16946 16975 17162 17002 16862 16869 17219 16887 16950 16949 16874 17147 16965 16889 17290 17055 17185 16966 17046 17112 17041 17289 17178 17103 17139 17260 16986 17000 17105 17390 17331 17098 17297 17052 17089 17373 17264 16871 17199 17190 17124 17382 16925 17159 17062 17372 16944 17173 17388 16885 17254 17187 17278 16934 16901 17231 17295 16932 16893 17025 17100 16878 16955 17360 16921 16922 16838 16876 16865 16926 16856 16928 16930 17333 17018 17363 17277 16968 17024 17210 17172 17251 17197 16911 16978 17049 16919 17338 17179 17259 17248 17351 17238 17165 17048 17206, and 17158.  H3000WD: 17154 17310 17113 17072 17163 17236 17067 17067 17107 17346 17252 17126, and 17379.
  • Classification du dispositif
    Radiology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution -- USA including states of AL, AK, AZ, AR, CA, CO, CT, DE, FL, DC, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, MT, NE, NV, NH, NJ, NM, NY, NC, ND, OH, OK ,OR, PA, PR, SD, TN, TX, UT, VT, VA, WA, WV, and WI and countries of AUSTRALIA, BELGIUM , BRASIL, CANADA, CHINA, COLUMBIA, CZECH REPUBLIC, DENMARK, ECUADOR, FINLAND, FRANCE, GEORGIA, GERMANY, INDIA, INDONESIA, ISRAEL, ITALY, JAPAN, KOREA, MEXICO, NETHERLANDS, NEW Zealand, NORWAY, POLAND, PUERTO RICO, RUSSIA, SOUTH AFRICA, SPAIN, SWEDEN, SWITZERLAND, TAIWAN, THAILAND, TURKEY, UKRAINE, UNITED KINGDOM.
  • Description du dispositif
    GE Healthcare Infinia Hawkeye(R) 4, Model numbers: || H3000WC || H3000WD || Intended use: To perform general Nuclear Medicine imaging procedures for detection of radioisotope tracer uptake in the patient body, using a variety of scanning modes supported by various acquisition types and optional imaging features designed to enhance image quality in Oncology, Cardiology, Neurology and other clinical diagnostic imaging applications.
  • Manufacturer
    GE Medical Systems, LLC

Manufacturer

GE Medical Systems, LLC
  • Adresse du fabricant
    GE Medical Systems, LLC, 3000 N Grandview Blvd, Waukesha WI 53188-1615
  • Société-mère du fabricant (2017)
    General Electric Company
  • Source
    USFDA