New research has confirmed the link between bisphoshonates, such as Fosamax, and atypical femur fractures, a type of thigh fracture that occurs spontaneously, without any major leg injury. The study, published in the Archives of Internal Medicine, also found that the risk of atypical thigh fractures increases the longer a ...
National law firm, Parker Waichman LLP, just filed a lawsuit on behalf of the estate of a Kentucky man who developed bladder cancer and subsequently died, allegedly due to the use of diabetes drug, Actos. The lawsuit names Takeda Pharmaceuticals America, Inc., Takeda Pharmaceuticals USA, Inc., Takeda Pharmaceuticals North America, ...
Johnson & Johnson’s Ethicon Inc. division revealed yesterday that it will end sales of its Gynecare Prolift device and three other transvaginal mesh products. The plan to stop selling the four products was set forth in a letter filed by the company in the Ethicon transvaginal mesh multidistrict litigation ...
Early results from the largest study to date to compare Pradaxa and warfarin indicate that in a real-world setting, Pradaxa causes more complications than decades-old warfarin. The preliminary study results were announced last week, during the 2012 Thrombosis and Hemostasis Summit of North America.
A national law firm is not satisfied with the way the U.S. Food & Drug Administration (FDA) has handled warnings regarding Actos (pioglitazone) bladder cancer risks. In a statement published today, Parker Waichman LLP called on the FDA to compel Takeda Pharmaceuticals, the maker of the type 2 diabetes drug, ...
Krazy Glue Packaging is Misleading, Class Action Alleges A consumer fraud class action lawsuit has been filed against Elmer’s Products Inc. alleging that its Krazy Glue packaging is misleading. The suit alleges that the packaging, which is large and opaque, … Continue reading →
Owners of Dodge RAM 2500 and 3500 trucks filed a class-action lawsuit against automaker Fiat Chrysler and engine-maker Cummins Inc., alleging that the two companies knowingly deceived consumers and regulators about illegally high levels of diesel emissions. In 2012, the … Continue reading →
Ten children who used what has been described as homeopathic teething tablets have died and another 400 adverse events have been tied to the tablets according to reports to the U.S. Food and Drug Administration (FDA). The agency warned caregivers … Continue reading →
A $55 million judgment awarded in a 2016 talcum powder lawsuit has been upheld, according to an Order dated September 9th. The Missouri 22nd Judicial Circuit Court for St. Louis City denied Johnson & Johnson’s post-trial motions which included a … Continue reading →
On August 23, a request was made by Johnson & Johnson (J&J) to dismiss claims of conspiracy, fraud, misrepresentation and warranty claims relating to its talcum powder, saying that the claims were not specific enough. The motion was filed in … Continue reading →
A class action lawsuit has been filed against KAS Direct LLC d/b/a Babyganics alleging that the company’s baby products are not actually organic. Plaintiffs allege that the products are falsely represented and alleges that Babyganics engaged in unlawful, unfair, deceptive … Continue reading →
A class-action lawsuit has been filed against Wen Hair Care products and their distributor, Guehy-Renker, for allegedly causing hair loss (alopecia). More than 21,000 complaints have been received against Wen, sold by Hollywood hairstylist Chaz Dean. The U.S. Food and … Continue reading →
Numerous complaints of hair loss, bald spots, rashes, and itching after using Wen hair cleansing conditioner prompted the U.S. Food and Drug Administration (FDA) to issue a safety alert. As of July 7, 2016, the agency has received 127 direct … Continue reading →
The U.S. Food and Drug Administration (FDA) has issued a recent public safety statement regarding IVC filters and potential health risks connected to their use. The FDA approved IVC filters in 1979. At that time, only 2,000 devices were implanted. … Continue reading →
According to a new study by Consumer Reports over 40 percent of the 60 sunscreens tested by experts fall short of their SPF numbers printed on the product’s label. The U.S. Food and Drug Administration (FDA) requires all sunscreens to … Continue reading →