Health Canada has become the most recent national drug regulator to issue a warning about Actos and bladder cancer. Last month, the agency warned that interim results from a 10-year-study indicated that patients taking Actos for more than a year faced an increased risk of bladder cancer. Health Canada also ...
Medtronic Inc.’s published studies for its Infuse bone graft product may have downplayed serious side effects, according to an analysis published last year in The Spine Journal. The study, which drew on U.S. Food & Drug Administration (FDA) documents and other data sources, suggests that up to half of ...
Roughly 1,000 people in Australia have had to undergo revision surgeries because of failed DePuy ASR hip implants. According to TheAge.com, DePuy Orthopaedics has heard from more than 4,000 people in Australia and New Zealand seeking help with the recalled metal-on-metal hip replacement devices.
Another lawsuit has been filed over adverse Plavix side effects. The lawsuit, filed by national law firm Parker Waichman LLP, alleges that the blood thinner, Plavix (clopidogrel), caused an Oklahoma man to suffer from multiple stomach bleeds.
A new study is raising more concerns about the safety of commonly used antidepressants, including selective serotonin reuptake (SSRI) inhibitor antidepressants. Investigators who conducted the study, which is published in the journal Frontiers in Psychology, posit that increased knowledge of the negative effects of SSRIs and other antidepressants could reduce ...
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 →