As a partner with D'Arcy Johnson Day, Andrew has been involved in some of the nation’s most high-profile cases and investigations. His practice includes serious automobile accidents, medical malpractice, wrongful death and product defect cases.
Side effects of Nexium, Prilosec and other blockbuster heartburn and acid reflux medications have been linked to a risk of acute kidney injury, chronic kidney disease and potentially kidney failure. A product liability lawsuit filed over the side effects of Nexium, Prilosec and Prevacid indicates…
Jury selections began this week in the first bellwether trial for thousands of Xarelto lawsuits pending throughout the federal court system, involving allegations that the drug makers failed to adequately warn about the gastrointestinal bleeding risks associated with the controversial new-generation
The size and structure of aging Americans is changing. According to the U.S. Census Bureau, the nation will experience considerable growth in its older population as baby boomers continue to enter their golden years. This growth in elderly individuals is increasing the demand and need…
According to a recent court filing, Johnson & Johnson now faces talcum powder lawsuits brought by more than 4,000 plaintiffs nationwide, with most involving allegations that years of using Johnson’s Baby Powder or Shower-to-Shower caused adult women to develop ovarian cancer. There are large dockets
The U.S. Food and Drug Administration has cited local generic drug giant Mylan for “significant violations” of manufacturing regulations at a plant in Nashik, India, according to a warning letter released by the agency Tuesday. The FDA conducted inspections at the plant from Sept. 5-14…
Recently, the drug company Mylan issued a voluntary recall in seven countries for the EpiPen. The initial recall of the emergency allergy product didn’t include the US, but Mylan has issued a new recall which not only includes EpiPens sold in the US, but also…
Ford Motor Company is recalling 570K vehicles for a variety of safety issues. The recall for over half a million of its vehicles are due to a variety of problems including engine fires and doors that fly open on their own. The first recall covers…
The side effects of a Mirena IUD caused a Pennsylvania woman to develop severe migraine headaches, blurred vision and a host of other health problems associated with the buildup of fluid pressure around her brain, according to allegations raised in a lawsuit recently filed against…
AstraZeneca’s prescription medication Onglyza, used in the treatment of Type 2 diabetes, may cause an increase in certain cardiovascular events, and could even result in death. Onglyza received FDA approval on July 31st, 2009, and is used to help control high blood sugar in patients…
The New Jersey Department of Health says that over 30 patients contracted infections at the Osteo Relief Institute in Wall Township after receiving injections for knee pain management. The facility closed on March 7th after patient complaints about bacterial infections. Monmouth County Health Offic
The FDA has provided additional information to patients and medical providers regarding the recall of the Comprehensive Reverse Shoulder Implant initiated by Zimmer Biomet on December 20, 2016. The recall has been designated a “Class 1” recall, which reflects the highest classification available to
According to the findings of a new research, very few nursing homes follow the recommended isolation precautions for residents with multi-drug resistant infections, which may place other nursing home residents at risk of the serious and potentially life-threatening “superbug” infections. About 2 m