Stryker has recalled the two products, “given the potential risks associated with fretting and corrosion at the modular neck junction,” according to the news release. In addition to the recall, the company will cease global distribution of the products.
More Articles on Orthopedic Devices:
CSU Researchers Develop Joint Implant Material
SpineGuard Announces 20k Spine Procedures Performed With PediGuard Devices
Southwest NeuroSpine Institute Purchases Mazor Robotics’ Renaissance System
At the Becker’s 32nd Annual Meeting: The Business and Operations of ASCs, taking place October 29-31 in Chicago, ASC leaders, surgeons and healthcare executives will explore strategies to drive growth, enhance operational performance, navigate reimbursement challenges and prepare for the future of ambulatory surgery. Apply for complimentary registration now.
