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.
