Fractures of the Zimmer Biomet Comprehensive Reverse Shoulder Implant Can Result In:
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Infection
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Loss of Shoulder Function
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Severe Pain
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Death
Frequently Asked Questions
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Why was the shoulder device recalled?
Zimmer Biomet recalled its comprehensive reverse shoulder system because cases were reported of the device fracturing more than expected. As a result, a number of complications were arising including infection, inability to use the shoulder, and even death.
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What are some complications of the shoulder device?
A number of complications have been reported, including but not limited to permanent loss of function of the shoulder, heightened risk of fracture, bone loss, infection, metal toxicity, fracture of the device, instability, weakness, and even death.
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What is an FDA Class I Recall?
The FDA issues recalls to remove dangerous and defective products from the market. A Class I is the most serious type of recall, issued when there is reasonable probability that the use or exposure to a product may lead to serious adverse health complications or in the worst cases, death.
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Why do I need an attorney?
Lawsuits can be long and complicated, and the outcome of a lawsuit can be greatly improved with the assistance of an experienced attorney. At Shaheen & Gordon, we believe that when someone has been seriously injured or lost their life due to a defective product, justice needs to be restored. We prepare every case as if it will go to trial and, if a case must be taken to court, we will not hesitate to go toe to toe with a large opponent or corporation. Rest-assured that when our clients’ rights and well-being have been compromised, we are willing to do whatever it take to help them receive full compensation.
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