WebStryker’s toll-free Patient Care Line can be reached by calling 1-888-317-0200 (U.S. and Canada only). The Patient Care Line is available from 8am–9pm EST, Monday through Saturday. Information about the Voluntary Recall What Patients Should Do Testing & Treatment Claims & Reimbursement Important information WebMako uses CT-based 3D modeling of the patient’s bony anatomy to provide you with a personalized surgical plan. Mako Total Hip enables surgeons to more accurately plan and place components, potentially reducing variability within the THA procedure and allowing for enhanced functional and clinical outcomes. 16-23.
Modular Neck Stem Voluntary Recall Information Stryker
WebA number of Stryker knee replacement implants have been recalled because of loosening, early wear, or faulty packaging and resulted in defective product lawsuits. Facing facts As of August 2024, there were nearly 2,000 Stryker hip and knee replacement lawsuits filed. Reasons for knee replacement device recalls WebMar 22, 2024 · MAHWAH, N.J., March 22, 2024 /PRNewswire/ -- Stryker's Joint Replacement Division announced today the introduction of the Insignia® Hip Stem, engineered to optimize patient fit and surgeon ease... memory process model
Recall - Robotic surgical cutting system may calculate incorrect ...
WebNov 25, 2024 · Recall Number: Z-0472-2024 REASON Stryker has discovered a characterization issue associated with the Mako Integrated Cutting System (MICS) Handpiece. WebMako Total Knee is for people with: Severe knee pain or stiffness resulting from: noninflammatory degenerative joint disease (including osteoarthritis, traumatic arthritis, … WebJan 10, 2024 · One company, Stryker, had to recall more than 200 models of their product as people reported bone fractures and metal poisoning after using the faulty medical devices. While the following is merely a brief list of defective medical devices, you can call your doctor to see if your device has been recalled. DePuy memory processing issues