Hernia Mesh failure requires additional surgery to repair damage caused by defective mesh
Lawsuits have been filed by thousands of people who were injured by hernia mesh patches and plugs made from 2006 through 2019.
Since 2010, the FDA has received over 2,800 reports of the Paragard device failures including
Many women have reported that the device can also break during the removal procedure and that the broken pieces must be painfully removed one by one with a complicated surgery to avoid organ damage.
Based on a congressional report, 1 in 3 people were abused in nursing homes in a short two-year study period.
Our Nursing Home Attorneys will review your case for FREE.
You could be entitled to compensation for the Abuse/Neglect suffered for medical bills and pain and loss!
You could be entitled to compensation for Roundup® /Cancer, medical bills, pain.
Bayer has announced a settlement after years of litigation from cancer patients who claimed Roundup® caused non-Hodgkin lymphoma and that Monsanto failed to adequately warn consumers of the risk.
Studies show 1 out of 4 IVC Filters fracture, potentially causing death.
A defective IVC filter can fracture and be carried away by the blood stream into the heart or lungs.
Most patients do not know if their IVC filter is defective or broken until it is too late.
About 30% - 40% of liver failure cases are linked to herbal or dietary supplements.
Unlike prescription or over-the-counter drugs, which must be approved by the FDA before they can be marketed, the FDA is not authorized to review dietary supplements for safety and effectiveness before they are sold.
Steering and Drive-Train Component Problems
Vanderhall sells three wheel vehicles that have engines and other components designed and manufactured for a four wheel automobile. Three wheel vehicles are classified as a motorcycle and therefore do not meet federal automotive requirements for safety.
Recent studies have shown that up to a quarter of patients who take Elmiron long-term suffer retinal damage, including vision loss.
In June 2020 the manufacturer of Elmiron updated its label with the FDA to warn physicians for the first time that long-term use of Elmiron has been reported to cause eye damage.
Penumbra Jet 7 Xtra Flex Catheter Lawsuit
In June 2019, the Jet 7 Xtra Flex Catheter received approval to be used in brain surgery procedures in the US. In October of 2020, there were increased reports of serious malfunctions of the device leading to injuries and death of patients.
On December 15, 2020, the FDA announced that Penumbra had issued an urgent recall of the Penumbra Jet 7 Xtra Flex Catheter.
The agency determined that levels of a cancer-causing chemical impurity (NDMA) can increase in the pills over time, or when the pills are stored above room-temperature. This means all over-the-counter and prescription-strength Zantac and ranitidine will no longer be sold in the U.S.
We accept cases for a wide-variety of personal injury claims including claims against manufacturers of prescription or over-the-counter drugs, medical device defects, other defective products, and negligence claims. Our Texas product liability lawyers accept cases from throughout the United States including: Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin and Wyoming.
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