Devices

Device Recall Allura XPER 10/10

  • Modèle / numéro de série
    FCO 72200124 and 72200125 for 1st phase FCO 72200133 for 2nd phase Equipment #'s: 103281, 103283, 505903, 506119, 530653, 532614, 533397, 536028, 536031, 536034, 536035, 536037, 536042, 536171, 536715, 536789, 536899, 537631, 537804, 538028, 538157, 538387, 538409, 538514, 538516, 539326, 539628, 540184, 540237, 541577, 541589, 541590, 542413, 542557, 542714, 543200, 543289, 543411, 543879, 543989, 544395, 544433, 545025, 545396, 545604, 545753, 545884, 545997, 546013, 546569, 547173, 547769, 547823, 547922, 548140, 548288, 549368, 549903, 551855, 554802, 554970, 555293, 555299, 555834, 41443647, 41443804, 41444647, 41444650, 41445448, 41445501, 41445538, 41455885, 41455897, 41455920, 41780160, 42057324, and 42064724.   Additional Equipment #s from phase 2- 10107, 101110, 101205, 557729, 557908, 41443609, 41445432, 41446024, 41446262, 41660520, 42046440, 42064058, 42394072, 42553772, 42625859, 42891704, 43043666, 43164789, 43173591, 43453735, 43848923, 43931292, 44028554, 44066424, 44193760, 44892370, and 47140511.
  • Classification du dispositif
    Radiology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution
  • Description du dispositif
    Allura XPER 10/10
  • Manufacturer
    Philips Medical Systems North America Co. Phillips
  • 1 Event

Fabricant

Philips Medical Systems North America Co. Phillips
  • Adresse du fabricant
    Philips Medical Systems North America Co. Phillips, 22100 Bothell Everett Hwy, Bothell WA 98021-8431
  • Source
    USFDA