Device Recall Ziehm Solo FD

  • Model / Serial
    S/N 52199, 52108
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    US Distribution to the states of : FL and CA. No devices listed in this recall where distributed any foreign /military/government consignees from the U.S.A.
  • Product Description
    Ziehm Imaging solo FD Mobile Fluoroscopic C-arm
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    Ziehm Imaging Inc, 6280 Hazeltine National Dr Ste 100, Orlando FL 32822-5114
  • Manufacturer Parent Company (2017)
  • Source
    USFDA