Complications from a Biomet Device?

Your Time Is Limited – Take Action Now by Requesting a Free Case Review

If you or a loved one have suffered health complications following a Zimmer Biomet shoulder device implant procedure, don’t delay in contacting Shaheen & Gordon, P.A., because you may have grounds to take legal action. In February of 2017, the FDA identified the Biomet Reverse Shoulder recall as Class I, which is the most serious recall possible, due to the severe complications the device has caused.

Common complications of the Zimmer Biomet shoulder device include:

  • Permanent Loss of Function
  • Heightened Risk of Fracture
  • Bone Loss
  • Infection
  • Metal Toxicity
  • Fracture of the Device
  • Instability or Weakness
  • Death

Shaheen & Gordon is currently filing lawsuits for the design, manufacture, and marketing of a defective medical device, failure to properly research the long-term success of the device, failure to provide adequate warnings about the risk of complications, and the misrepresentation of the safety of the device.

If you or your loved one received the implant anytime from 2008 to 2016 and have suffered serious complications, we urge you to contact our firm immediately. As a well-known and respected firm with millions of dollars in recoveries on behalf of our clients, you can be confident that we have the tenacity, resources, and skills needed to help you and your family achieve the justice and results you deserve.

Always striving for efficiency, justice and success, you can trust that our team will do whatever it takes to right the wrongs that have been done to you and your family.