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Your Stryker Hip Implant Could Be Flawed: Important Research Information

According to an FDA Warning issued on November 28, 2007 and released to the public on January 15, 2008, some models of Stryker hip implants may be flawed. The FDA issued this warning to Stryker Corporation after conducting research and inspections of Stryker’s facility located in Mahwah, New Jersey.

Patients who have received a Stryker hip implant, including the Trident Hemispherical and Trident PSL cups have experienced problems such as fractures, pain, wear particles, fragments and broached bones resulting in bone fractures.

Also, some Stryker implant patients with ceramic bearing components have also experienced squeak-like noises when walking or engaging in other activities.

The Defective Drugs and Medical Devices unit at our firm is uniquely qualified to take on cases involving faulty implants. Hip replacement patients with Stryker implants or those who have undergone replacement surgeries, or who have suffered emotional injuries due to malfunctioning implants, should fill out the form below for a free case evaluation.

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Please complete the following questionnaire:

Name
Email
Phone Number
Were you implanted with a Stryker Hip Implant?
If yes, when?
Has your implant or related components failed to work properly?
If so, please describe.
Did you require surgery to fix the problem?
Additional Comments


see also:

News & Warnings Read the FDA Warning Letter re: Stryker Hip Implants.
FDA issues Warning Letter re: Stryker Hip Implants. Get the info here.

Learn More Stryker Was Warned Hip Implants Were Defective - Our lawyers are aware
Our Defective Drug Lawyers are reviewing Stryker Hip Implant cases

FREE Legal Review Free Lawsuit Evaluation from Experienced Stryker Hip Implants Lawyers
FREE Lawsuit Evaluation on Stryker Hip Implants Injuries

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