Device Recall PRO 2 Device

  • Model / Serial
    Model Numbers: PRO235, PRO240, PRO245, PRO250  Lot Numbers: 67102 to 68418
  • Product Classification
  • Device Class
    2
  • Implanted device?
    Yes
  • Distribution
    Devices were distributed in the following states: AL, AR, AZ, CA, CO, FL, GA, ID, IL, IN, KS, KY, LA, MD, MI, MN, MO, MS, NC, NE, NY, OH, OK, PA, SC, TN, TX, UT, VA, VT, & WI. Devices were distributed in the following countries: Austria, Germany, Netherlands, Poland, Sweden, Switzerland and United Kingdom.
  • Product Description
    AtriClip" LAA Exclusion System with preloaded Gillinov-Cosgrove" Clip - A single PRO2 device is packaged in a conventional thermoformed polyethylene terephthalate glycol (PETG) tray with a Tyvek¿ lid. A single-walled non-corrugated box completes the single unit package. Six (6) single unit PRO2 devices are packaged into one (1) corrugate shipper box.
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    AtriCure, Inc., 7555 Innovation Way, Mason OH 45040-9695
  • Manufacturer Parent Company (2017)
  • Source
    USFDA