Device Recall Juno

  • Model / Serial
    Serial Numbers: 10110770 11030805 11070848 11070845 11070849 11030806 11090864 11110900 12020982 114087 12030999 12061020 12041003 12061014 12061018 12081040  :
  • Device Class
    Not Classified
  • Implanted device?
    No
  • Distribution
    US Nationwide Distribution including the states of AL, CA, CO, CT, IL, MD, MI, MO, NY, OH, PA
  • Product Description
    Juno DRF , X-ray system, diagnostic, Fluoroscopic, general-purpose || Model: 70920 || Product Usage: || Universal R/F, general use
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    Philips Healthcare Inc., 3000 Minuteman Road, Andover MA 01810
  • Manufacturer Parent Company (2017)
  • Source
    USFDA

2 devices with a similar name

Learn more about the data here

  • Model / Serial
    P/N 709020
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    US Distribution to the states of: AZ, AL, CA, CO, CT, DC, FL, IA, IL, IN, MI, MD, MS, MA, MO, NY, OH, PA, UT, TN and TX.
  • Product Description
    Juno DFR X-ray system
  • Manufacturer
  • Model / Serial
    10110770 11030805 11030806 11070845 11070848 11070849 11090864 11110900 12020978 12020982 12030999 12041003 12061014 12061018 12061020 12081040 12091074 12101104 12121186 12121187 13031215 13101263 14021301 14031313 14041321 14051332 14071353 14081359 14091368 14091371 14121400 14121403 15021426 15031440 15041444 15091473 15091478 15101484 15101487
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    AL AZ CA CO CT DC FL IA IL IN LA MA MD MI MN MO MS NJ NY OH PA Puerto Rico TN TX UT WI
  • Product Description
    Juno DRF; Model: 709020 || Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.
  • Manufacturer