Retiro De Equipo (Recall) de Device Recall EasyDiagnost Eleva xray systems

Según U.S. Food and Drug Administration, este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en United States que fue producido por Philips Medical Systems North America Co. Phillips.

¿Qué es esto?

Una corrección al equipo o acción de retiro tomada por el fabricante para abordar un problema con un dispositivo médico. Los retiros (recalls) ocurren cuando un dispositivo médico está defectuoso, cuando puede poner en riesgo la salud, o cuando simultáneamente está defectuoso y puede poner en riesgo la salud.

Más información acerca de la data acá
  • Tipo de evento
    Recall
  • ID del evento
    50742
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0353-2009
  • Fecha de inicio del evento
    2008-12-10
  • Fecha de publicación del evento
    2009-09-24
  • Estado del evento
    Terminated
  • País del evento
  • Fecha de finalización del evento
    2012-08-17
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
  • Notas / Alertas
    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.
  • Notas adicionales en la data
    Angiographic X-Ray System - Product Code JAA
  • Causa
    Tube failure occurs involving fluoroscopy of large patients and a partial failure of the grid switch.
  • Acción
    An Electronic Product Radiation Warning, dated October 2008, was sent to customers. The letter identified the problem and under what circumstances that it could occur; the actions that should be taken by the customer/user to prevent risks for patients or users; and the actions planned by Philips to correct the problem. Further information or support concerning the issue could be obtained by contacting Bob Pettis at 425-487-7469 or the Philips Call Center at 800-722-9377. Firm FCO tracking numbers 72200107, 72200108, 72200111, 72200112, 72200117, 72200118, 72200119, 72200122, 72200123, 72200124, 72200125, 72200129, 72200142, 7989980, 7080085, 70600034, 70600035, 72200132, 72200133, 72200137, 72200138, 72200140 and 72200141. C & R # 1217116-10/20/08-016C

Device

  • Modelo / Serial
    FCO 70600034 and 70600035 Equipment #'s 102174, 102549, 102551, 103515, 103522, 103523, 104471, 104877, 105118, 105323, 105392, 105482, 105640, 105678, 105775, 105921, 105922, 105954, 504611, 504751, 504826, 504935, 504941, 505003, 505015, 505062, 505255, 505349, 505653, 505671, 505749, 505798, 505871, 506076, 506199, 506207, 506210, 506211, 506233, 506238, 506248, 506250, 506270, 506272, 506273, 506553, 506554, 506844, 506845, 519117, 519122, 519125, 519128, 519152, 519550, 519562, 519575, 519773, 519776, 519826, 519879, 519900, 520045, 520409, 520798, 521153, 521654, 521658, 521684, 521771, 521942, 522028, 522073, 522178, 522193, 522219, 522255, 522271, 522399, 522470, 522480, 530573, 530607, 530797, 530798, 530806, 531832, 532137, 532139, 532174, 532177, 532360, 532397, 532398, 532426, 532477, 532842, 532971, 533234, 533451, 533491, 533558, 533565, 533766, 533770, 533771, 533914, 533918, 534434, 534596, 534599, 534600, 534615, 534647, 534675, 534803, 534850, 534867, 535255, 535365, 535378, 535436, 535437, 535757, 535765, 535771, 535785, 536179, 536522, 536636, 536938, 536984, 536985, 537087, 537179, 537518, 537761, 537796, 537863, 538328, 538451, 538477, 538519, 538759, 538812, 538814, 539095, 539101, 539237, 539291, 539377, 539378, 539379, 539519, 539527, 539529, 539530, 539557, 539590, 540163, 540187, 540459, 540624, 540788, 541011, 541054, 541075, 541078, 541093, 541494, 541614, 541721, 541872, 542205, 542589, 542593, 542829, 542849, 543136, 543144, 543224, 543241, 543249, 543275, 543369, 543415, 543619, 543620, 543660, 543771, 543803, 544113, 544228, 544236, 544297, 544341, 544648, 544654, 545120, 545231, 545234, 545244, 545391, 545452, 545710, 545746, 545783, 545824, 545948, 545951, 546029, 546490, 547243, 547297, 547304, 547655, 547657, 547744, 547758, 547759, 547936, 547937, 548021, 548302, 548382, 548559, 548784, 549008, 549080, 549416, 550197, 550313, 550804, 550960, 551616, 551645, 551759, 551980, 552363, 552364, 552917, 552965, 552966, 553013, 553172, 553224, 553230, 553275, 553441, 553448, 553491, 553563, 554483, 554581, 554641, 554721, 554769, 555052, 555269, 555458, 555524, 556984, 557177, 557259, 557272, 558596, 41443633, 41443799, 41443813, 41443842, 41444437, 41444555, 41444600, 41444676, 41445431, 41445443, 41445458, 41445483, 41445650, 41445745, 41445752, 41445942, 41445982, 41445990, 41446006, 41446012, 41446214, 41446312, 41446777, 41487231, 41658234, 41658273, 41704405, 41862667, 41974615, 42029462, 42067090, 42122305, 42122745, 42162796, 42163516, 42225532, 42336983, 42379116, 42382599, 42456354, 42456355, 42617047, 42638020, 42823862, 42850557, 42880751, 42892412, 42892413, 43208952, 43452066, 43453550, 43613284, 43671121, 43680073, 43691433, 43708636, 43971738, 43989706, 44049065, 44065204, 44202885, 44340799, 44605123, 44621189, 44651312, and 4654127.
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution
  • Descripción del producto
    EasyDiagnost Eleva x-ray systems
  • Manufacturer

Manufacturer

  • Dirección del fabricante
    Philips Medical Systems North America Co. Phillips, 22100 Bothell Everett Hwy, Bothell WA 98021-8431
  • Source
    USFDA