Device Recall PKG, ATRAUMATIC FORCEPS, SINGLE ACTION

  • Model / Serial
    42714 43489 43490 143175 143176 143452 143453 340645 444574 641197 643520 647411 7108579 740242 840911 844136 848107 941058 942653 943254 943440 945124 1040231 1040393 1042255 1042649 1042650 1043453 1046589 1046699 1046906 1141173 1141190 1141384 1143126 1145283 1145682 1145977 1146679 1243100 1243539 1245517 1246171 1340193 1340476 1340586 1341582 1342389 1343704 1344285 1345531 1440912 1441963 1442257 1442810 1443396
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution - USA (nationwide) and Internationally to Algeria, Argentina, Australia, Bolivia, Brazil, Canada, Chile, China, Colombia, Costa Rica, Ecuador, France, Germany, Greece, Guam, Guatemala, India, Italy, Japan, Jordan, Kuwait, Latin America, Malaysia, Mexico, Morocco, Netherlands, New Zealand, Peru, Philippines, Poland, Portugal, Puerto Rico, Romania, Saudi Arabia, South Africa, South Korea, Spain, Sweden, Switzerland, Taiwan, Turkey, United Arab Emirates, United Kingdom, and Venezuela.
  • Product Description
    PKG, ATRAUMATIC FORCEPS, SINGLE ACTION, P/N 0250080310. || Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio frequency (RF) ports which allow them to be used for electrosurgery. Laparoscopic surgical manual instruments are designed to be used endoscopically through cannulae to perform cutting, grasping, dissecting, retracting, and manipulating functions. This device does not sustain or support life.
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    Stryker Endoscopy, 5900 Optical Ct, San Jose CA 95138-1400
  • Manufacturer Parent Company (2017)
  • Source
    USFDA