from the U.S. Food and Drug Administration website**: Intercharm Inc. Issues A Nationwide Voluntary Recall Of Slim Forte Slimming Capsules Lot 20100604 And Lot 20100928, Slim Forte Slimming Coffee Lot 20100903, And Meizitang Botanical Slimming Softgel Exp. 12.23.2011 Weight Loss Capsules Found To Contain Sibutramine Contact: Intercharm Inc. 323-876-7441 FOR IMMEDIATE RELEASE - July 25, 2011 - Intercharm Inc., is recalling Slimforte Slimming Capsules, Slimforte Slimming Coffee, and Botanical Slimming Soft Gel to the consumer/user level. FDA laboratory analyses found the products to contain … [Read more...]
Hair Removal Service Not Protected Under Health Care Liability Act
from Texas Lawyer Bioderm Skin Care LLC v. Sok Tx. App. Dist. 5 Kerry P. Fitzgerald Justice 05-10-00044-CV 06-28-2011 OPINION Before Justices Morris, O'Neill, and FitzGerald Opinion By Justice FitzGerald Appellee Veasna "Sandee" Sok sued Bioderm Skin Care, LLC ("Bioderm") and Quan Nguyen, MD, seeking to recover damages for burns she suffered during a laser hair removal procedure at Bioderm. Bioderm and Nguyen contend Sok’s claims are health care liability claims and are subject to Chapter 74 of the Texas Civil Practice and Remedies Code. Accordingly, they moved to … [Read more...]
What’s Fair Is Fair: Rise in FDCPA Cases Offers Opportunities for Lawyers
From The Texas Lawyer, July 18, 2011 With the economic downturn, the number of consumer credit-related suits filed in U.S. District Courts in Texas has steadily increased over the past five years. In 2005, 81 such cases were filed in Texas, according to PACER, the federal courts' online filing system. But in 2010, that number rose to 390. The trend is on track to continue this year. From Jan. 1 to June 30, 2011, the number of consumer credit-related cases filed in Texas' U.S. District Courts totaled 263, compared to 190 for the same period in 2010, PACER shows. The numbers include consumer … [Read more...]
FDA Reports Cancer Risk from Osteoporosis Drugs
An FDA Safety Alert issued today warns that taking oral osteoporosis drugs (“bisphosphonates”) may cause an increased risk of esophageal cancer. This category of drugs includes Fosamax, Actonel, Boniva, Atelvia, Didronel, and Skelid. Esophageal cancer and other esophageal problems have been reported in connection with use of the drugs, and the FDA is reviewing data from published studies to determine whether a link exists. The FDA posted the following recommendation in its Safety Alert: “Patients should talk with their healthcare professional about the benefits and risks of taking oral … [Read more...]
Chrysler Recalls Three Models of Ram trucks
News Source: The Kansas City Star - July 13, 2011 Chrysler Motor Corporation announces a recall nearly 250,000 Ram pickups because of a faulty part in the steering system which can cause loss of control. This recall affects Chrysler’s top-selling vehicle and covers about 243,000 Ram 1500, 2500 and 3500 pickups ranging from year models 2008 through 2011. The National Highway Traffic Safety Administration reports that a part near the left front wheel can fracture and risk potential crash of the vehicle. … [Read more...]
Toyota Plans Recall of Hybrid SUVs
Toyota Hybrid SUVs May Suddenly Lose Power or Stop Completely by By Jonathan Welsh of The Wall Street Journal - June 29, 2011 2011 Toyota Highlander Toyota Motor Corp. said today it will recall about 82,200 hybrid sport-utility vehicles to correct an electronic problem that could cause the vehicles to lose power or stop running completely. The car maker said the recall includes about 45,500 Highlander Hybrid and 36,700 Lexus RX 400h models from the 2006 and 2007 model years and sold in the U.S. The company said no other Toyota or Lexus vehicles are involved in the recall. Toyota … [Read more...]
G.M. Recall for Inaccurate Shift-Lever Reading
Recall of Almost 6,800 Pickups By CHRISTOPHER JENSEN of The New York Times 2011 GMC Canyon, one of the models affected in a recall by General Motors. General Motors is recalling almost 6,800 pickups from the 2011 model year because they might roll away even when the automatic transmission’s selector appears to be in Park. The automaker also said it recalled 739 pickups and sport utility vehicles because of a possible loss of steering. The pickups affected by the shift-lever issue are the Chevrolet Colorado and GMC Canyon equipped with the 4-speed automatic and either the … [Read more...]
Copyright Dispute Over Tattoo not to Block Movie
May 24, 2011 By Debra Cassens Weiss From ABAJournal.com: Judge Rules ‘Hangover II’ May Be Released, Despite Copyright Dispute over Tattoo The show must go on, according to a federal judge ruling in a copyright dispute involving a tattoo. The Hangover: Part II was allowed to open this week after U.S. District Judge Catherine Perry refused to issue an injunction barring its release, according to The Wrap and Hollywood, Esq. Warner Bros. issued a statement saying it is gratified by the decision. Perry ruled in a suit by tattoo artist S. Victor Whitmill, who claims an actor in the movie … [Read more...]
Volkswagen Recalls Certain New Jettas To Fix Wiring
from The Wall Street Journal Blog Volkswagen of America Inc. said today it is recalling certain 2011 Jetta models to fix a potential problem with the wiring of its anti-theft system and horn. The car maker says the recall affects 71,043 Jettas built between March of 2010 and March of 2011. The company says the problem stems from the a fuse that protects the car’s anti-theft alarm and the converter box that operates the windshield wipers and headlights. Under certain rare circumstances a short circuit in the horn can cause the lights and wipers to stop working, which could increase the … [Read more...]
J&J recalling more Tylenol from closed plant
Reported in Reuters by Lewis Krauskopf -- Johnson & Johnson said it was recalling more than 700,000 bottles or packages of Tylenol and other consumer medicines made at a now-closed plant, the latest in a litany of recalls by the company. J&J’s McNeil Consumer Healthcare unit recalled one lot of Tylenol 8 Hour Extended Release Caplets, or 34,056 bottles, from retailers, the company said. The company cited a musty odor that has prompted many other J&J recalls. The product was made at its Fort Washington, Pennsylvania plant before J&J closed the facility in April … [Read more...]
