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
- Metal Toxicity
- Fracture of the Device
- Instability or Weakness
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.