Devices

Device Recall Philips

  • Modèle / numéro de série
    Allura Xper with release R8.2,
  • Classification du dispositif
    Radiology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide, Canada, Algeria Argentina Australia Austria Bahrain Bangladesh Belgium Brazil Brunei Darussalam Bulgaria CHILE China Colombia Croatia Cuba Cyprus Czech Republic Denmark Dominican Republic Ecuador Egypt Finland France French Polynesia Georgia Germany Greece Honduras Hong Kong Hungary Iceland India Indonesia Iran Ireland Israel Italy Japan Jordan Kazakhstan Kenya Korea, Republic of Lebanon Lithuania Macedonia Malaysia Malta Mexico Morocco Myanmar Nepal Netherlands New Caledonia Norway Oman Pakistan Palestine, State of PERU Philippines Poland Portugal Qatar R¿union Romania RUSSIAN FEDERAT Russian Federation Saudi Arabia Singapore Slovakia South Africa Spain Sri Lanka Sweden Switzerland Taiwan Tanzania Thailand Tunisia Turkey Ukraine United Arab Emirates United Kingdom Uruguay Uzbekistan Viet Nam
  • Description du dispositif
    Allura Xper with release R8.2: Allura Xper FD10, 722026; Allura Xper FD10/10, 722027; Allura Xper FD20, 722028; Allura Xper FD20/10 biplane, 722029; || Allura Xper FD10 OR Table, 722033; Allura Xper FD10/10 OR Table, 722034; || Allura Xper FD20 OR Table, 722035; Allure Xper FD20/20 , 722038; Allura Xper FD20/20 biplane OR Table, 722039; Allura Xper FD20/15, 722058; Allura Xper FD20/15 OR Table, 722059
  • Manufacturer
    Philips Electronics North America Corporation
  • 1 Event

Fabricant

Philips Electronics North America Corporation
  • Adresse du fabricant
    Philips Electronics North America Corporation, 3000 Minuteman Rd, Andover MA 01810-1032
  • Société-mère du fabricant (2017)
    Philips
  • Source
    USFDA

229 dispositifs médicaux avec un nom similaire

En savoir plus sur les données ici

Device Recall Philips Bucky Diagnost FS
  • Modèle / numéro de série
    Site numbers: 504495, 105355, 104447. The firm uses site numbers instead of serial numbers.
  • Classification du dispositif
    Radiology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    The firm distributed to three medical facilities in Florida, New York and California.
  • Description du dispositif
    Bucky Diagnost FS Part number 9890-010-83651
  • Manufacturer
    Philips Medical Systems Sales & Service Region No. America
Device Recall Philips Digital Diagnost VE
  • Modèle / numéro de série
    Site numbers: 82652, 82681, 82723, 82730, 83073, 85495, 85696, 85697, 85698, 86222, 86382, 86383, 86987, 86988, 100572, 100806, 101933, 102030, 102100, 102115, 102116, 102117, 102489, 102539, 102596, 102713, 102717, 102719, 102787, 102905, 103109, 103165, 103262, 103271, 103272, 103436, 103437, 103438, 103439, 103453, 103511, 103778, 103893, 103894, 103953, 103971, 103976, 104014, 104338, 104465, 104578, 104673, 104676, 104864, 104902, 104903, 104904, 104937, 104938, 105158, 105198, 105199, 105322, 105367, 105415, X1641, X1642, X1650, X1767, X1768. The firm uses site numbers instead of serial numbers.
  • Classification du dispositif
    Radiology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    The firm distributed to medical facilities nationwide.
  • Description du dispositif
    Digital Diagnost VE
  • Manufacturer
    Philips Medical Systems Sales & Service Region No. America
Device Recall Philips brand MX8000 IDT CT Scanner System
  • Modèle / numéro de série
    Serial Numbers: 2501 to 2554; 3006; 3008 to 3337.
  • Classification du dispositif
    Radiology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    The systems were installed at medical facilities located nationwide and worldwide.
  • Description du dispositif
    Philips MX8000 IDT CT Scanner System, 10 & 16 slice images.
  • Manufacturer
    Philips Medical Systems (Cleveland) Inc
Device Recall Philips brand Brilliance CT Scanner System
  • Modèle / numéro de série
    Serial Numbers: 2555 to 2568; 3335 to 3392; 9701 to 9725.
  • Classification du dispositif
    Radiology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    The systems were installed at medical facilities located nationwide and worldwide.
  • Description du dispositif
    Philips Brilliance CT Scanner System, 6, 10 & 16 slice images.
  • Manufacturer
    Philips Medical Systems (Cleveland) Inc
Device Recall Philips
  • Modèle / numéro de série
    Software versions A.02.00 and lower
  • Classification du dispositif
    Cardiovascular Devices
  • Classe de dispositif
    3
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide Foreign:Canada, Austria, Australlia, Belgium, China, Denmark, Finland, France, Germany, Israel, Italy,Kuwait, Latvia, Lebannon, Libya, Netherland,Norway, Portugal, Qatar, Russia, Singapore,South Africa, Spain, Switzerland, Sweden, Taiwan, Thailand,Tunisia, UK, United Arab Emirates, Yemen
  • Description du dispositif
    Philips Heartstart MRx Monitor/Defibrillator || Models: M3535A (Hospital Use) , M3536A (EMS Use)
  • Manufacturer
    Philips Medical Systems
224 en plus