On April 1, regulatory bodies in Ireland and the U.K. told physicians that no Magec device should be implanted until a review of the products has been completed.
In February, NuVasive issued an urgent field safety notice, recalling its Magec X spinal rods after the separation of an actuator end cap component was reported in 0.5 percent of the devices post-implantation.
The Health Products Regulatory Authority in Ireland and the Medicines and Healthcare Products Regulatory Authority in the U.K. will conduct an independent review of the Magec devices.
More articles on devices:
Physician group furloughs, layoffs, hours cut: economic responses to the pandemic
15 new COVID-19 cases linked to orthopedic practice in Alaska
Orthopedic surgeons among specialists called to treat COVID-19 patients in NYC
At the Becker's 23rd Annual Spine, Orthopedic and Pain Management-Driven ASC + The Future of Spine Conference, taking place June 11-13 in Chicago, spine surgeons, orthopedic leaders and ASC executives will come together to explore minimally invasive techniques, ASC growth strategies and innovations shaping the future of outpatient spine care. Apply for complimentary registration now.
