Category Archives: Consumer Fraud
Smith & Nephew’s Birmingham Metal-on-Metal Hip Replacement Device
Wright Medical Inc. took steps in to 2006 to convince the U.S. Food & Drug Administration (FDA) to reject pre-market approval of rival Smith & Nephew’s Birmingham metal-on-metal hip implant. Wright Medical, which makes two metal-on-metal hip replacement devices, the Conserve and the Lieneage device, filed a citizen petition ...
Sudden Death in Those Taking Bactrim Along with ACE Inhibitors or ARBs
Association between sudden death in those given Bactrim while already taking renin-angiotensin system blockers angiotensin receptor blockers (ARBs), heart medications.
FDA Urged to Ban Powdered Caffeine
Pennsylvania Senator Robert Casey has written to the Food and Drug Administration (FDA) to urge the agency to ban powdered caffeine, a dietary supplement.
Federal Judge Certifies Medtronic Infuse Shareholder Class Action Lawsuit
A shareholder lawsuit alleging Medtronic Inc. illegally promoted the off-label use of its Infuse bone growth product has been granted class action status by U.S. District Judge Paul Magnuson of Minnesota. According to a report from Law360.com, the Medtronic Infuse off-label promotion lawsuit was filed by several institutional investors on ...
Smith & Nephew Says Metal-on-Metal Hip Replacement Controversy Slowing Sales of Birmingham Hip Resurfacing System
Medical device maker Smith & Nephew has reported a drop in sales of its metal-on-metal hip implant devices. According to the company, hip implant sales were down 2 percent during the first quarter of 2012, largely because its Birmingham Hip Resurfacing System suffered from an association with other metal-on-metal hip ...
Actos, Avandia May Up Risk for Diabetic Macular Edema
A West Virginia man fitted with a metal-on-metal version of DePuy Orthopaedics’ Pinnacle Hip Implant System has filed suit against the company and its parent, Johnson & Johnson, alleging the device caused him to suffer pain and elevated cobalt levels. The Plaintiff is being represented by the national law ...
Actos Side Effects Lawyers Says Whistleblower Revelations Could Boost Bladder Cancer, Heart Failure Lawsuits
An attorney with a prominent personal injury law firm says an Actos whistleblower lawsuit filed earlier this year could strengthen legal claims alleging the type 2 diabetes medication caused some users to develop bladder cancer and heart failure.
Medtronic Sprint Fidelis Leads Vulnerable to Fracture after ICD Switch
Medtronic Sprint Fidelis leads are vulnerable to fracture following ICD switch, says a new study published in the June issue of the journal Heart Rhythm.
Scientist Calls for Federal Regulations for Fracking Pollution
Hydraulic fracturing (fracking) drilling should be governed by federal regulations because its pollution has no awareness of state boundaries.
Tennessee Resident Files Pradaxa Bleeding Lawsuit Following Cerebral Hemorrhage
A man from Tennessee has filed a lawsuit against the maker of Pradaxa, claiming that the blood thinner caused him to suffer a cerebral hemorrhage. The complaint alleges Boehringer Ingelheim Pharmaceuticals, Inc. concealed knowledge that Pradaxa can cause Serious, life-threatening bleeds, and did not warn that Pradaxa bleeding side effects ...Class Action Lawsuit Filed over Elmer’s Krazy Glue Packaging
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
Class Action Lawsuit Over Defective Dodge RAM Diesel Trucks
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
Homeopathic Teething Products May Be Tied to 10 Children’s Deaths and 400 Adverse Event Reports
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
J&J Talcum Powder Lawsuit Verdict Upheld, J&J Appeals
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
Johnson & Johnson Request Dismissal of Fraud Accusation on Talc Lawsuit
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
Class Action Lawsuit Filed over Babyganics
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
FDA Investigates Wen Hair Care Products
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
Wen Conditioner Hair Loss Complaints Prompt FDA Safety Alert
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
Public Scrutiny of IVC Filters Increase as Lawsuits Mount
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
Sunscreen Products Not Delivering SPF Levels as Labeled
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
