Stryker® Knee Replacement Lawsuits

Stryker knee implant painThe knee replacement devices manufactured by Stryker Orthopaedics have caused patients tremendous pain and injury, prompting many to undergo additional surgeries to correct these issues.

Despite Stryker’s products being touted as some of the best in the medical industry, the problems caused by these devices have sparked a number of Stryker knee implant lawsuits. Patients experiencing difficulty walking or pain related to their replaced knee should contact a medical professional immediately if they believe their Stryker device is faulty.

The class action lawyers at Gordon & Doner believe that victims of defective medical devices deserve justice. If you suffered injuries or required revision surgery because of a faulty Stryker knee replacement, you may be entitled to file a Stryker knee implant lawsuit.

Schedule a free case review by calling 1 (855) 722-2552.

Were Stryker Knee Replacements Recalled?

In 2012, the Food & Drug Administration (FDA) issued a class II recall on Stryker EIUS Unicompartmental knee systems. Reports from two National Joint Registries revealed the devices had a much higher than normal failure rate.

Stryker Orthopaedics sent “Urgent Product Recall” letters to all affected customers. The letters identified the product and detailed actions that should be taken by patients with the affected product.

Still, the company manufacturers many other types of knee replacement systems. The company has not issued an official recall on other knee replacement devices despite patients reporting complications and knee system failure.

This is not the first time Stryker Orthopaedics has been subjected to an FDA recall. The FDA first became aware of issues with Stryker products in January 2005 when knee implant patients reported serious complications, like extreme pain in the surgical area, squeaky joints, breaking or chipping of implant parts and difficulty walking. Some even suffered bone fractures, and many patients required revision surgery. In 2007, the FDA sent warning letters to Stryker in order to correct procedural failures in testing problematic components and documenting risk.

Should I File a Lawsuit?

Patients are sometimes unsure of the brand of knee replacement they received. Contact your surgeon to learn whether a Stryker knee was used in your surgery. If you experienced any of the following symptoms of knee replacement failure, you may wish to seek a qualified lawyer to file a claim:

  • Bone, joint, or muscle damage
  • Chronic pain
  • Fracturing of the device
  • Immobility
  • Infection
  • Inflammation
  • Instability
  • Joint swelling

Did you experience Stryker knee failure and have to undergo revision surgery? If so, you may be entitled to file a Stryker knee implant lawsuit. If you wish to consult with an attorney, the initial consultation with a lawyer at Gordon & Doner is free. Our team of attorneys can help you determine if you are eligible to file a lawsuit, and if so, how to proceed.

Live Chat with a representative to schedule a consultation today.

Contact a Stryker Knee Implant Lawyer Today

If you or a loved one has suffered an injury from a defective Stryker knee implant or were forced to undergo a revision surgery after being implanted with a recalled knee implant, you may be entitled to compensation.

Contact the Stryker knee implant lawsuit attorneys at Gordon & Doner today to schedule a free, no-obligation case evaluation to see if you have cause to file a lawsuit. Our attorneys are available to answer any questions you may have regarding Stryker knee implant recalls and can offer advice on the best course of action to take in pursuing compensation for your losses.

Fill out a contact form or call 1 (855) 722-2552 to speak with an attorney.

 

Gordon & Doner - For The Injured®

1 (855) 722-2552

Gordon & Doner, P.A.

4114 Northlake Blvd
Palm Beach Gardens, FL 33410
Phone: 561-333-3333

Gordon & Doner - Davie

10650 Florida 84 #210
Davie, FL 33324
Phone: 754-333-3333

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Stuart, FL 34994
Phone: 772-333-3333

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