Events

Rappel de Device Recall GE Innova

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 Datex - Ohmeda, Inc.

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
    49538
  • Classe de risque de l'événement
    Class 2
  • Numéro de l'événement
    Z-1521-2008
  • Date de mise en oeuvre de l'événement
    2008-05-19
  • Date de publication de l'événement
    2008-09-30
  • Statut de l'événement
    Terminated
  • Pays de l'événement
    United States
  • Date de fin de l'événement
    2016-06-30
  • Source de l'événement
    USFDA
  • URL de la source de l'événement
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=73763
  • 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
    Solid State X-Ray Imager - Product Code MQB
  • Cause
    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).
  • Action
    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
  • Modèle / numéro de série
    Systems Id: 8613100, 0910163013, 4103323100, 4103623100, 5034353100, 7083333100, 7278253100, 8019643100, 82416040010, 082416040016, 082416040017, 082416050002, 082416070004, 082416100008, 82416120005, 082416120006, 082416130013, 0002581738X, 06074VAS01, 201541LAB2, 214324INNOVA2, 24516572980IN, 309691P3100, 310423INNOVA1, 313593IC1, 313593IC2, 314525SACL2, 314768SMCL3, 318448INNOVA2, 318449INNOVA2, 409899LAB3, 413447CATH, 413540IN1, 417269SCLD, 502587LAB4, 518525LAB1, 540953INNOVA, 561266IN31, 563421CATHLAB8, 573815BCR1, 600130VA01, 601553CL3, 602239LAB4, 602239LAB6, 602266LAB2, 603778ECL1, 608524NOVA, 615338CV2, 615769SKYCV2, 619340VA8, 619482INNOVA1, 619541INNOVA31, 619552INNOVA1, 702616INNOVA, 7028803100A, 713794LAB7, 713794LAB9, 714966INNOVA, 718283INNOVA3, 724773C1, 731422CV1, 732294INOV, 765453INNOVA1, 770991CL3, 773792CL3100, 773NORWG3100, 803329CL31, 808547QCV2A, 812238LIB1, 812283IN31, 812482INNOVA, 815599FHN3100, 817433HSW3100, 83INNOVA1188379, 850678IN3100, 904202CATH3, 908522LAB1, 928779INNOVA1, 936266CL1, 956389INN31, 956698INN31, 956994INN1, 956994INN2, 973971LAB3, A5108239, A5203215, BPINNOVA2, BPINNOVA3R, DK1066VA01, FHORLCL1, H1420VAS04, HC1536XR04, IQ1083VA01, IR1747VA01, LB1160XR07, LV4012VA01, M2848425, M2970614, PL1622VA01, RU1156VA01, RU1482VA02, RU1550VA01, RU2457VA01, TT-2586581-CO, YV0022, YV0026, YV0036.
  • Classification du dispositif
    Radiology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    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.
  • Description du dispositif
    GE Healthcare Innova 3100 Digital Fluoroscopic Imaging (Cardiovascular Imaging System)
  • Manufacturer
    Datex - Ohmeda, Inc

Manufacturer

Datex - Ohmeda, Inc
  • Adresse du fabricant
    Datex - Ohmeda, Inc, Po Box 7550, Madison WI 53707
  • Source
    USFDA