Recall Alert For Stryker Device Used in Spinal Fusions

On May 30, 2013, the FDA has issued a Class 1 recall (their most serious level of alert) of a Stryker implant device used in the upper spine and which has been shown to have a significant failure rate of one of its components. This failure may lead to serious injury, the need for replacement surgery, and even in some cases the risk of death.
For more information about this recall and what you need to know, please click here. The lawyers of the Ruth Law Team have experience in dealing with products liability issues in general and failed medical devices in particular. If you have questions or concerns, you may also get answers by calling us at 1-888-783-8378.