Stryker Lawsuit Infromation
You’ve should have received a letter from your doctor stating:
I am writing this letter to you because I have been informed by Stryker Orthopaedics, the manufacturer of your total hip prosthesis, that this prosthesis had been recalled.
A copy of the patient letter from Stryker Orthopaedics is enclosed for your information.
Recently, Styker has contracted surgeons who have used this prosthesis. They have recommended intermittent blood testing and possible imaging studies for ongoing evaluation of the prosthesis. Based upon their recommendations, I think that it would be appropriate to do these studies intermittently as long as this prosthesis is in place.
From their correspondence, they have begun reimbursing patients for testing, treatment, revision surgery, if necessary, and other costs relating to this voluntary recall, to manage requests for reimbursement of costs relating to the voluntary recall of the Rejuvenate Modular Neck Hip Stem.
If you have already contacted Stryker to submit a claim, Broadspire should contact you. Otherwise, to submit a claim and learn more about the claims process, you should call 1-888-317- or go to www.AboutStryker.com/ModularNeckStems, on the internet.
If you have further questions, please feel free to contact my office. I will do my best to help you with this difficult situation.