Device Recall CIVCO SBRT System, REF MTSBRT001L

  • Model / Serial
    M105110, M108810, M109210, M110470, M110500, M110510, M115630, M128700, M128710, M128720, M137600, M137610, M148780, M148790, M148800, M177910, M177920, M177930, M177940, M177950, M177960, M196700, M196710, M196720, M200120, M200130, M200140, M226740, M226750, M226780, M228640, M230110, M239340, M239350, M245100 and M258280
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution - USA ( nationwide) including the state of PA. and countries of: Canada, China, England, Israel, Italy, Japan, Korea, The Netherlands, Russia, Spain, Sweden, Switzerland and Turkey.
  • Product Description
    CIVCO SBRT System, REF MTSBRT001L, containing CIVCO Pro-Lok Platform, REF MTSBRT002. Firm name on label is CIVCO, Orange City, Iowa || Product Usage: The recalled product is intended to support and aid in positioning a patient during radiologic and other medical procedures.
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    Civco Medical Instruments Inc, 102 1st St S, Kalona IA 52247-9589
  • Manufacturer Parent Company (2017)
  • Source
    USFDA