Device Recall CIVCO ProLok Platform, REF MTSBRT002

  • Modèle / numéro de série
    M074130, M092920, M115600, M143230, M165570, M188350, M191650, M207130, M208340, M213570, M218300, M230730, M248840, M248850 and M268010
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    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.
  • Description du dispositif
    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

Fabricant

  • Adresse du fabricant
    Civco Medical Instruments Inc, 102 1st St S, Kalona IA 52247-9589
  • Société-mère du fabricant (2017)
  • Source
    USFDA