The Stryker Wingspan Stent System is designed to open up narrow arteries in the brains of individuals who have experienced repeated strokes. When it is used on patients who do not meet the usage criteria outlined by the FDA, however, it can have life-threatening or…
On Nov. 28, 2018, Stryker recalled its Tritanium posterior lumbar (PL) cage. Stryker’s reason for doing so, according to the FDA’s website, is that “the surgical technique is being updated to caution against misuse due to reports of cage fractures occurring intraoperatively and postoperatively.” In…
We are thrilled to report a jury in Hartford, Connecticut just returned a $542,645 compensatory award to our deserving clients: $42,645 for past medical expenses and $500,000 in non-economic/pain and suffering damages. The same jury indicated punitive damages are warranted to punish Boehringer Ingel
As consumers of modern medicine, we rely on the Food and Drug Administration (FDA) to inform us of the risks and complications associated with medical drugs and devices on the market. Unfortunately, this is often not the case. A recent Kaiser Health News investigation revealed…
Recently, a federal jury ordered Monsanto to pay $80 million to 70-year-old Edwin Hardeman, who got diagnosed with cancer after using their weed killer for 26 years. The weed killer in question, Roundup, is a glyphosate-based herbicide that Hardeman regularly used on his 56-acre property…
Recently, a federal jury in Indianapolis awarded $3 million to a woman who had serious medical complications caused by a defective inferior vena cava (IVC) filter. This verdict is noteworthy because it is the first bellwether trial to result in a win for the injured…
Today, many thousands of consumers have filed lawsuits against hernia surgical mesh implant manufacturers. Big name pharmaceutical companies like C.R. Bard, Johnson & Johnson/Ethicon, Atrium and others are the focus in these lawsuits for the debilitating medical side effects that resulted from their
Hernia surgical mesh implants are used to reduce hernia recurrence and provide support to tissue that is weakened or damaged because of a hernia. Hernias occur when an organ, intestine, or fatty tissue breaks through the wall of whatever is containing it, and can happen…
When an elderly individual suffers from a pulmonary embolism (PE), approximately one in six of them receive inferior vena cava (IVC) filters to decrease their risk of having subsequent PE. PE occurs when an artery in the lungs becomes blocked by a blood clot, which…
With thousands of reported side effects, the blood thinning drug Xarelto has been controversial since its initial approval for medical use in 2011. Nevertheless, Johnson & Johnson (J&J) submitted a Supplemental New Drug Application on Dec. 14 for Xarelto to be used as a preventative…
The FDA recently issued a warning dissuading customers from using Rhino male sexual enhancement products, which are unregulated supplements typically found for sale at gas stations and convenience stores. This warning comes after the discovery that many Rhino supplements contain unlisted ingredients
The FDA recently announced plans to overhaul its dated medical device approval system. The system, which has been in place since the 1970s, has been criticized for years due to its approval of over 95 percent of medical devices to be put on the U.S.…
