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For 109 years in the State of Florida, juvenile offenders were sent to Arthur G. Dozier School for Boys if the Court found they committed a crime or violated terms of juvenile probation. The school was in Mariana, Florida. According to an investigation by the
Tampa Bay Times, the children housed at the facility were between the ages of 5 and 20 years old.
Frequently, these children were first time offenders who had committed non-violent offenses, like shoplifting or trespassing. For decades, the State of Florida removed troubled youth from their parent’s care and sent to them to the state-run reform school where they would be committed for extended periods of time.
The subject of six lawsuits filed in three states, paraquat is widely used in the agricultural industry and, sadly, often causes illnesses to those least able to care for themselves:.
Until recently, Florida has had a Personal Injury Protection (PIP) insurance system, also known as “no-fault insurance.” The intention of PIP was to provide injured drivers immediate.
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Although “faulty” doesn’t necessarily mean “defective” or “dangerous,” product liability law does indeed hold manufacturers and others liable for producing dangerous products that cause injury. Product liability claims in Florida can be long and complicated, primarily due to the task of finding those parties that can be sued.
Who Can Be Sued For Product Liability in Florida?
Generally speaking, claims may be brought against any person or entity within the chain of design, manufacture, distribution, and sales of defective or dangerous products.
If you or a loved one has been injured or even killed because of a defective product, including a defective medical device, let an experienced Florida product liability attorney help you with these complicated claims.
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The U.S. Food and Drug Administration (FDA) is warning patients and healthcare providers of a “higher than expected risk” of failure in Stryker Scandinavian Total Ankle Replacement (STAR) devices. According to the FDA, the polyethylene component of Stryker’s STAR ankle replacement device is prone to breaking “as early as three to four years after implantation,” potentially necessitating surgery to repair or replace the device.
The FDA’s warning is based on the agency’s review of post-approval studies and adverse event reports. Based on its review, the FDA is warning that the risk of failure may be present in all Stryker STAR ankle replacement devices regardless of when they were manufactured or surgically implanted.