Endopath Probe Plus II, Right Ange Electrode, 5 mm shaft, 34 cm length, hollow tip electrode.

  • Model / Serial
    Lot C4DD4K, C4DJ5E, C4DK9M, and C4DN5E.
  • 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, Right Ange Electrode, 5 mm shaft, 34 cm length, hollow tip electrode, Product Code EPS03.
  • Manufacturer
  • 1 Event

Manufacturer

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