COVID-19 has upended life worldwide. This includes the legal system in Southern Arizona, which has faced court closures and delays, as well as restrictions on visits to attorneys. Challenges in receiving prompt and thorough medical attention, along with staffing problems at insurance companies, have also impacted the speed with which personal injury claims are resolved.…
On Wednesday, April 1, 2020, the U.S. Food and Drug Administration requested that manufacturers recall all prescription and OTC ranitidine drugs from the market immediately. The agency has determined that an impurity increases over time, particularly in warm storage temperatures, resulting in unacceptable exposure to the carcinogen NDMA. While some samples tested did not contain…
Personal injury lawyers strive to prove deliberate negligence or malicious intent in product liability lawsuits. Medical device manufacturers have a duty to conduct rigorous safety tests prior to releasing a product to market and to communicate all known risks to consumers. Determining what breast implant manufacturer Allergan did or didn’t know is at the center…
The unbearable pain of arthritis, hip fracture, ankylosing spondylitis, or bone dysplasia drives more than 300,000 Americans to seek hip replacement surgery each year. Patients with limited mobility turn to artificial hip technology after hearing promises that they can regain their full range of motion and quality of life again. However, for every 100…
The Centers for Disease Control reported that in 2019, more than 25% of U.S. teens used e-cigarettes. One of those teens recently filed a federal lawsuit against vape products manufacturer, Juul, alleging that the company used misleading advertising and promotional efforts that were directly responsible for his nicotine addiction. Many Juul lawsuits have followed and…
Truvada maker Gilead Sciences, Inc. has recently become the target of over 1,000 lawsuits alleging bone loss and related injuries. However, the company is facing a new lawsuit of a different sort – and from an unlikely party. On November 6, 2019, the United States, on behalf of the Department of Health and Human Services,…
In 2009, Uloric (active ingredient febuxostat) became the first prescription gout medication to gain FDA approval in 40 years. Doctors were quick to prescribe the new blockbuster drug, which has generated $1.9 billion in sales for manufacturer Takeda Pharmaceuticals within the last five years alone. Then, in February 2019, the use of this medication…
Earlier this month, the Superior Court of California ruled that personal injury lawsuits filed against Gilead Science, Inc. over its drug tenofovir disoproxil fumarate (TDF) can proceed. The company had attempted to dismiss the cases, which allege that HIV/AIDS medications based on TDF cause permanent kidney and bone damage. The court rejected all but one…
Across the U.S., over 1 million people undergo surgery to repair hernias annually. The majority of hernia repairs are done by reinforcing the affected areas with a man-made synthetic mesh. According to the U.S. Food and Drug Administration (FDA), 33% of patients report adverse events with hernia mesh. These complications, which often manifest as severe…
3M Combat Arms earplugs were standard-issued to thousands of service members deployed to Iraq and Afghanistan from 2003 to 2015. However, the manufacturer was sued by the U.S. government and competitor Moldex-Metric Inc. when defects were discovered that could cause tinnitus ringing in the ears and hearing impairment. The Veterans Benefits Administration treats over a…