Endopath Probe Plus II, Spatula Electrode, 5mm shaft, 34 cm length, hollow tip electrode

  • Model / Serial
    Lot C4DK34 and C4DK9L.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    The recalled product was distributed throughout the United States and to foreign consignees including Argentina, Australia, Austria, Bahrain, Brazil, Canada, China, Colombia, Czech Republic, Dominican Republic, Ecuador, France, Germany, Greece, Hong Kong, Hungary, India, Indonesia, Israel, Italy, Japan, Korea, Lebanon, Malaysia, Mexico, Netherlands, New Zealand, Pakistan, Peru, Philippines, Poland, Portugal, Puerto Rico, Saudi Arabia, Slovenia, South Africa, Spain, Sweden, Switzerland, Taiwan, Thailand, Turkey, United Kingdom, Uruguay, Venezuela.
  • Product Description
    Endopath Probe Plus II, Spatula Electrode, 5mm shaft, 34 cm length, hollow tip electrode, Product Code EPS02.
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    Ethicon Endo-Surgery Inc, 4545 Creek Rd, Cincinnati OH 45242-2803
  • Manufacturer Parent Company (2017)
  • Source
    USFDA