The FDA issued a patient safety alert regarding Equinoxe Shoulder System joint replacement devices manufactured by Exactech between 2004 and August 2021 due to a defect with the packaging.
Stryker is recalling 143 units of its Triathlon total knee system, according to a March 6 notice from the FDA. The recalls were initiated because of issues affecting the inner blister and outside sterile blisters of the implant packaging.
Medtronic Neurosurgery issued a Class I recall affecting 45,176 Duet external drainage and monitoring system catheter tubing following 26 reported injuries. The recall impacts five product models, according to a March 7 FDA alert. The recall was initiated on Jan. 22.
At the Becker's 23rd Annual Spine, Orthopedic and Pain Management-Driven ASC + The Future of Spine Conference, taking place June 18–20 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.
