Events

Rappel de Device Recall CT/e and HiSpeed X/i computed Tomography systems

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
    50528
  • Classe de risque de l'événement
    Class 2
  • Numéro de l'événement
    Z-2224-2009
  • Date de mise en oeuvre de l'événement
    2008-12-01
  • Date de publication de l'événement
    2009-09-18
  • Statut de l'événement
    Terminated
  • Pays de l'événement
    United States
  • Date de fin de l'événement
    2016-01-27
  • Source de l'événement
    USFDA
  • URL de la source de l'événement
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=75703
  • 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
    System, x-ray, tomography, computed - Product Code JAK
  • Cause
    During internal testing, ge healthcare has recently determined that the collimator used on our ct/e and hispeed x/i families of computed tomography systems does not comply with the specific requirements in united states title 21 of the code of federal regulations, and iec 60601-1-3, related to leakage radiation from the diagnostic source assembly, which includes the collimator. the excess leak.
  • Action
    GE Healthcare issued an "Important - Electronic Product Radiation Warning" to affected customers. GE Healthcare field service representative will perform a field corrective action on all affected units. All potential users of the device should be made aware of the notification and the information contained. For further information, contact GE Healthcare at 1-800-437-1171 (US) or by contacting your local GE Healthcare service manager.

Device

Device Recall CT/e and HiSpeed X/i computed Tomography systems
  • Modèle / numéro de série
  • Classification du dispositif
    Radiology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution -- UNITED STATES (AL, AZ, AR, CA, CT, DC, FL, GA, IL, IN, KS, KY, LA, MD, MA, MI, LMN, MS, MO, NE, NJ, NM, NY, NC, OH, OK, PA, PR,SC, SD, TN, TX, VA, WA, WV and WI), ALGERIA, ANTIGUA, ARGENTINA, AUSTRALIA, AUSTRIA, AZERBAIJAN, BELGIUM, BENIN, BOLIVIA, BOSNIA & HERZEGOVINIA, BRAZIL BULGARIA, BYELORUSSIAN, CAMERON, CANADA, CHILE, CHINA, COLOMBIA, CONGO, COSTA RICA, CROATIA, CYPRUS, CZECH REPUBLIC, DENMARK , DOMINICAN REPUBLIC, ECUADOR, EGYPT, EL SALVADOR, ESTONIA, FINLAND, FRANCE, GEORGIA, GERMANY, GREECE, GUADELOUPE, GUATEMALA, GUYANA, HONDURAS, HONG KONG, HUNGARY, ICELAND, INDIA, INDONESIA, IRAN, IRELAND, ISRAEL, ITALY, IVORY COST, JAPAN, JORDAN, KAZAKHSTAN, KOREA, KUWAIT, LATVIA, LEBANON, LIBYAN ARAB JAMAHIRIYA, LITHUANIA, , MACEDONIA, MALAYSIA, MALTA, MARTINIQUE, MAURITANIA, MAURITIUS, MEXICO, MOROCCO, NETHERLANDS, NEW ZEALAND, NICARAGUA, NIGER, NIGERIA, NORWAY, OMAN, PAKISTAN, PANAMA, PARAGUAY, PERU, PHILIPPINES, POLAND, PORTUGAL QATAR, ROMANIA, RUSSIAN F=FEDERATION, SAUDI ARABIA, SINGAPORE, SLOVAK IA, SOUTH AFRICA, SPAIN, SUDAN, SWEDEN, SWITZERLAND , SYRIA ARAB REPUBLIC, TAIWAN, THAILAND, TRINIDAD & TOBAGO TUNISIA, TURKEY,, UGANDA, UKRAINE, UNITED KINGDOM, URUGUAY, VENEZUELA, VIETNAM, YEMEN and YUGOSLAVIA.
  • Description du dispositif
    GE Healthcare CT/e and HiSpeed X/i, families of computed tomography Systems with Gantry. || The CT/e and HiSpeed X/i families CT Scanner Systems are indicated for head and whole body X-ray Computed Tomography 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