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DEATH IN GASTRIC BYPASS SURGERY RESULTS IN WRONGFUL DEATH MEDICAL MALPRACTICE LAWSUIT

Bruce Roberts — Fri, 23 Mar 2007 13:32:40 GMT

The mother of a Houston woman who died after undergoing gastric bypass surgery filed a wrongful death medical malpractice lawsuit against the surgeon, Dr. Younan Nowzaradan, and Houston Community Hospital.

In her wrongful death lawsuit the mother claims that the doctor and the hospital did not sufficiently warn her daughter who weighed 520 pounds that the surgery would be especially risky for women of her weight.

According to the mother her suit was prompted when she learned that another overweight woman had died from a massive heart attack two weeks after Dr. Nowzaradan had performed gastric bypass surgery on her. According to the Houston Chronicle the mother's medical malpractice wrongful death lawsuit was prompted when she learned of the second woman's death.

The suit was prompted, in part, by the death of Renee Williams, the 841-pound Austin woman who died earlier this month from a massive heart attack, nearly two weeks after Nowzaradan performed gastric bypass surgery on her.
Since her daughter's death, Colleen Shepherd had "been going back and forth in terms of whether to pursue legal action, but she now has a renewed vigor," after the media coverage of Williams' death,...
Nowzaradan said he didn't know Tina Shepherd had died. He saw her at least once after the surgery, but she failed to follow up when his office repeatedly called her at home.

Originally posted at InjuryBoard by Bruce Roberts

Three Injured In Three-Vehicle Accident

Chrissie Cole — Thu, 01 Oct 2009 12:36:00 GMT

Three people were sent to the hospital on Wednesday following a three-vehicle accident on U.S. Highway 79.

The accident happened just after 4 p.m. about a mile west of State Highway 110, according to Lt. Mike Terry with the Jacksonville Fire Department.

While the cause of the accident is unknown, Lt. Terry said the crash involved a Ford Bronco, small pickup truck and a four-door car.

When officials arrived to the accident scene, one vehicle was in a ditch and the other two were in the middle of the highway.

Three of the four people involved in the crash were taken to the hospital. The extent of their injuries is not known. However, two of them had to be extricated using the Jaws of Life.

Originally posted at InjuryBoard by Chrissie Cole

Woodville Woman Killed In Rollover Accident

Chrissie Cole — Sun, 22 Mar 2009 10:07:00 GMT

A Woodville woman was killed Saturday night in a single-car accident when she was ejected from the vehicle, according to the Texas Department of Public Safety.

The woman, 59, was heading south on FM 92 just after 10:00 p.m. when she lost control of her vehicle and ran off the roadway on a curve to the left. The vehicle rolled over several times and she was ejected.

She was declared dead at the scene.

Car Accident Statistics

Every 12 minutes a person dies because of a car accident and every 14 seconds, a car accident results in an injured victim.

The majority of car accident victims are the drivers, followed by the passengers, pedestrians and lastly cyclists.

It is estimated that there are more than 6 million car accidents annually in the U.S.

Originally posted at InjuryBoard by Chrissie Cole

Deere & Company Recalls John Deere Tractors Due to Collision Hazard

Jenny Albano — Wed, 16 Jan 2008 15:52:03 GMT

Deere & Company, in conjunction with the CPSC, is recalling about 5,400 John Deere Compact Utility Tractors due to a collision hazard.

The forward drive pedal can get stuck, posing a risk of loss of control and injury to the operator and bystanders. Deere & Company has received seven reports of incidents. No injuries have been reported.

The recalled product has a model number that is 3203, which is located on the side of the tractor. The recall includes the following serial numbers:
LV3203H000001 through LV3203H000010
LV3203H190001 through LV3203H193434
LV3203H393093
LV3203H394001 through LV3203H396669

The serial number is located above the right front wheel on the tractor's frame. The recalled tractors were available at John Deere dealers across the U.S. from September 2007 to December 2007. The product was made in the United States.

For more information on this subject, please refer to our section on Defective and Dangerous Products.

Originally posted at InjuryBoard by Jenny Albano

Sweetwater Valley Farms, Inc. Recalls Southern Cheddar Jack Volunteer Special Cheese

Jenny Albano — Sun, 25 Nov 2007 20:22:43 GMT

Sweetwater Valley Farms Inc., in conjunction with the FDA, is recalling its Southern Cheddar Jack Volunteer Special Cheese because it may be contaminated with Listeria monocytogenes. Pregnant women, young children, the elderly, and people with weakened immune systems are most vulnerable to Listeria. Symptoms of Listeriosis include, but are not limited to, fever, fatigue, nausea, vomiting, and diarrhea. Treatment typically involves antibiotics.

Southern Cheddar Jack Volunteer Special Cheese, Lot Number 539 was distributed in 7, 10, 15 ounce, and 5 pound blocks and through retail stores in Tennessee, North Carolina, Georgia, Virginia, Maryland, and Alabama. The product was also distributed to 48 contiguous states in gift baskets marketed by the firm's website.

The cheese was distributed from September 19, 2006 to November 18, 2007. So far no illnesses have been reported to the company. The problem was discovered by the Tennessee Department of Agriculture during a routine sampling. Sweetwater Valley Farms has stopped distributing this product while it investigates the cause of the contamination problem.

For more information on this subject, please refer to our section on Defective and Dangerous Products.

Originally posted at InjuryBoard by Jenny Albano

Third Recall for Mattel Because of Lead-Tainted Toys

Jenny Albano — Thu, 06 Sep 2007 01:00:15 GMT

Mattel has announced another recall on toys, which has been the third recall in less than five weeks. All the recalled toys have been pulled from the shelves because of excess lead in the surface paint.

This worldwide recall involves 11 different toys, including eight pet and furniture playsets sold under the Barbie brand and three Fisher-Price toys -- two GeoTrax toys and a Big, Big World bongo set. No Barbie dolls are affected. A total of 844,000 toys are involved, about two-thirds of which were sold in the U.S. The toys were all made in China by several different vendors.

Robert Eckert, chairman and chief executive of El Segundo, Calif.-based Mattel, said that there may be more recalls because the company has increased investigations into the Chinese factories that manufacture their goods and intensified production checks. The company spent more than 50,000 investigating its vendors and testing their toys. As a result of these investigations a number of manufacturers will no longer be making toys for Mattel.

Here is the list of recalled toys:

-Fisher Price Big Big World 6-in-1 Bongo Band toys, sold from July, 2007 to Aug. 2007.

-Fisher-Price Geo Trax Locomotive Toys, sold from Sept. 2006 through Aug. 2007

-Various Mattel Barbie Accessory Toys, sold from Oct. 2006 through Aug. 2007:

-Barbie Dream Puppy Houseâ„¢ (lead paint on dog)

-Barbie Dream Kitty Condoâ„¢ Playset (lead paint on cat)

-Barbie Table and Chairs Kitchen Playset (lead paint on dog, chip platter, dinner plates)

-Barbie Bathtub and Toilet Playset (lead point on cat)

-Barbie Futon and Table Living Room Playset (lead paint on cat)

-Barbie Desk and Chair Bedroom Playset (lead paint on dog)

-Barbie Couch & Table Living Room Playset (lead paint on purse)

For more information on this subject, please refer to our section on Defective and Dangerous Products.

Originally posted at InjuryBoard by Jenny Albano

Cloud's Tuna and Egg Salad Sandwiches Recalled Due to Contamination

Jenny Albano — Wed, 08 Aug 2007 13:45:57 GMT

CFS Operating Ltd. is recalling 4219 units of Cloud's Tuna Salad Sandwiches and Egg Salad Sandwiches because they may be infected with Listeria monocytogenes, which is an organism that can cause serious infections in children, elderly people, and those with weak immune systems and may even cause death. For healthy adults the infection may cause high fevers, headaches, stiffness, nausea, abdominal pain, and diarrhea. For women that are pregnant the infection can cause miscarriages and stillborns.

The sandwiches were available in convenience stores in East Texas, West Louisiana, and Southwest Arkansas. The problem was discovered when FDA officials during normal sampling and inspections.

These sandwiches are labeled with "Cloud's Tuna Salad" and "Cloud's Egg Salad" located on the product label. The product was packaged in flexible plastic film and plastic wedges. Recalled products are as follows:
Cloud's Tuna Salad Sandwich on White Bread, 5 oz., date code 62607-72507
Cloud's Egg Salad Sandwich on White Bread, 5 oz., date code 41907-72507

So far no illnesses have been reported to CFS. The company is working with the FDA to rectify the problem.

For more information on this subject, please refer to our section on Defective and Dangerous Products.

Originally posted at InjuryBoard by Jenny Albano

TB Patient from Arkansas Flees Hospital

Jenny Albano — Thu, 12 Jul 2007 12:17:26 GMT

Franklin Greenwood, 50, was placed under isolation at the University of Arkansas for Medical Sciences hospital on June 29. He was seen coughing up blood outside the building for traffic court. After being held at the hospital for a few days Greenwood broke a window and fled the hospital. Hosptial authorities kept a civilian worker outside his room so he would be unable to leave.

Arkansas health officials said that the form of tuberculosis that Greenwood had was treatable, unlike Georgia lawyer Andrew Speaker, but it was still contagious. A UAMS spokesperson Leslie Taylor stated that the hospital had no authoirty to hold the man against his will, but still left a guard outside his room. State police were told to keep an eye out for Greenwood.

Originally posted at InjuryBoard by Jenny Albano

Food and Drug Administration to Strengthen Warnings for Antidepressant Drugs

Bruce Roberts — Fri, 01 Jun 2007 14:47:18 GMT

The FDA (Food and Drug Administration) approved the strongest possible warnings for antidepressants to warn patients and physicians that the drug could increase the risk of suicidal thinking and behavior in adults 18 to 24 years of age.

The action comes after a Food and Drug Administration committee recommended the warning after finding small increases in suicidal thoughts, and behaviors by young adults taking commonly used antidepressants. According to the study approximately 5 of every 1,000 patients ages 18 to 24 were at increased risk. There are some 16,000,000 people in the United States who take antidepressants and about 8 percent are people under age 25.

"The risk is small but the risk is real, and it is something that needs to be paid attention to," Dr. Thomas Laughren, director of the FDA's division of psychiatry products, said during a news conference.

In an unusual move, Laughren said the new labels would carry both a warning and positive information on the benefits of antidepressants.
The labels would emphasize weighing the risks associated with the drugs against the danger of failing to treat depression and other psychiatric disorders that contribute to suicide

Originally posted at InjuryBoard by Bruce Roberts

Oxycontin Manufacturer Agrees to Plead Guilty and Pay Fine of $600,000,000

Bruce Roberts — Mon, 28 May 2007 16:36:30 GMT

The company that makes the narcotic painkiller OxyContin and three current and former executives of Purdue Pharma, the company that markets OxyContin pled guilty in Federal Court to criminal charges that they misled doctors, federal regulators and patients as to the addictive nature as to the prescription drug, OxyContin. OxyContin is a powerful, long-acting narcotic that provides relief of severe pain for periods up to 12 hours.

When OxyContin was first released on the market, its manufacturer claimed that its time-release formulation would pose a lower threat of abuse and addiction than other painkillers including Percocet or Vicodin. This claim became part of an aggressive marketing campaign to get doctors like general family practitioners with little training in pain management and/or addiction behavior to begin prescribing the drug.

The scheme worked. By 1996, annual sales of OxyContin had reached $1,000,000,000.00. Unfortunately with increasing sales came evidence of increasing addiction and overdoses.

Federal officials said that internal Purdue Pharma documents show that company officials recognized even before the drug was marketed that they would face stiff resistance from doctors who were concerned about the potential of a high-powered narcotic like OxyContin to be abused by patients or cause addiction.
As a result, company officials developed a fraudulent marketing campaign designed to promote OxyContin as a time-released drug that was less prone to such problems. The crucial ingredient in OxyContin is oxycodone, a narcotic that has been used for many years. But unlike other medications like Percocet that contain oxycodone along with other ingredients, OxyContin is pure oxycodone, with a large amount in each tablet because of the time-release design.
The drug has proven to be valuable in treating serious, long-lasting pain.

Originally posted at InjuryBoard by Bruce Roberts