Zimmer Biomet Recalls ROSA One 3.1 Brain Application Due to Error in Software

Date:10/29/2021

Product type: Medical Devices

  • ROSA One 3.1 Brain Application
  • Product Codes and Lot Numbers: See Recall Database Entry 
  • Devices Recalled in the United States: 119
  • Distribution Date: December 1, 2019 to August 31, 2021
  • Date Initiated by Firm: September 22, 2021

US-FDA Link: https://www.fda.gov/medical-devices/medical-device-recalls/zimmer-biomet-recalls-rosa-one-31-brain-application-due-error-software