Atlanta, Georgia Personal Injury Lawyer
Salmonella is a very dangerous food borne bacteria which is well known for being dangerous to people, and has been responsible for numerous cases of food poisoning. Symptoms include severe diarrhea, and especially in children or the elderly, it can lead to complications which pose serious health risks. While not normally fatal, salmonella is responsible for deaths every year within the United States.
Products being recalled include:
T. Marzetti Southwest Ranch Veggie Dip, 15.5- ounce (UPC 70200 52004) Best By dates: APR2010F, APR2810F, MAY1610F, MAY3110F, JUN0610F, JUN1410F, JUN1910F
T. Marzetti Fat Free Southwest Ranch Veggie Dip, 13- ounce (UPC 70200 52033) Best By dates: MAY1610F, MAY3010F, JUN0810F, JUN1210F, JUN2510F
T. Marzetti Spinach Veggie Dip, 15-ounce (UPC 70200 52059) Best By dates: APR1910F, MAY0910F, JUN0710F
Great Value Ranch Chip Dip, 16 ounce (UPC 78742 43099) Best By dates: 042810F, 050810F, 052910F, 053010F, 053110F, 060410F, 060510F, 061110F
The Great Value Ranch Chip Dip is mostly distributed through Walmart and Sam's Club, while the T. Marzetti varies are distributed widely through a variety of supermarket chains.
Consumers who have purchased these products should either discard them, or return them to the store where they were purchased for a refund. Because of the potential of salmonella poisoning, these products are possibly dangerous and should not be eaten. T. Marzetti can be contacted by those who have questions at: 800-427-0147
State Agriculture Commissioner Tommy Irvin's office announced this recall last week, hopefully before there could be serious consequences from the tainted food. I have written before about the damaging consequences of salmonella contamination and poisoning, and while this does not seem to be on the same scale as last year's peanut recall, it is still a serious recall. It would be a mistake to understate how greatly this disease can affect people's lives. Exposure to unclean food is one of the more common methods of contracting salmonella, along with exposure to contaminated water and exposure to feces.
If you or a loved one has been injured by a recalled or defective product, it is important contact a Georgia accident lawyer as soon as possible. You may be entitled to compensation. Call MLN Law at 404-531-9700 to schedule a free consultation.
Labels: consumer products, Georgia accident lawyer, Georgia injury lawyer, georgia product liability attorney, product liability, product recall
So far this month, the FDA has posted announcements of several separate incidents where known and potentially dangerous allergens were not disclosed on a product's packaging. I could say that we here in Georgia are lucky that none of the recalls are likely to affect us locally; however, two of these incidents involve products distributed in more than one state. In the case of the allergy alert which Pierino Frozen Foods Inc. issued on its Jumbo Shells with Cheese, the recalled product was sold in stores in Michigan, West Virginia, Ohio, Pennsylvania, Indiana, Colorado, Texas, Kentucky, North Carolina, Virginia, and Florida - essentially across the entire country.Pierino Frozen Foods Inc. failed to include eggs as a potential allergen on the Jumbo Shells with Cheese's packaging, putting people with allergies or intolerances to eggs in danger of reactions. So far, there has only been one confirmed allergic reaction to the undeclared eggs, thankfully mild, but this mistake could easily have resulted in a far more serious, potentially even fatal reaction in someone with severe allergies to egg.
Roughly 4 percent of adults in our country suffer from food allergies, and something like 6 to 8 percent of children. Food intolerances, which are less dangerous, are even more common. In people who have food allergies, exposure to even trace amounts of the allergen can result in an immune response. Symptoms of an allergic reaction could be from discomfort in the form of digestive problems or hives, to life threatening if the victim suffers from anaphylaxis.
Anaphylaxis is an allergic reaction which affects the whole body, and can cause a person's airways to constrict. Also called anaphylactic-shock, anaphylaxis is relatively rare, but exceptionally dangerous, especially if left untreated.
The FDA requires manufacturers to list warnings for some of the most common potential allergens. While people can develop allergies to nearly any food, potentially, a few common foods make up the vast majority of life threatening allergies in adults and children. These allergens include: peanuts, tree nuts, fish, shellfish, eggs, milk, wheat and soy. While it is not required by the FDA, many manufacturers also list potential allergens which other products may have come in contact with.
These precautions may seem extreme to people who do not themselves have experience with severe food allergies, however they can be life saving for people who live with them. The most effective treatment for these people is nothing less than entirely avoiding the food that they are allergic to, making clear labels and warnings nothing less than a manufacturer's responsibility to its consumers.
If you or a loved one has been injured by a recalled or defective product, contact a Georgia personal injury lawyer immediately. You may be entitled to compensation. Call MLN Law at 404-531-9700 to schedule a free consultation.
Labels: atlanta product liability lawyer, consumer products, food allergies, georgia product liability attorney, product liability, product recall
The Agriculture Commissioner's office in a release which came out last week that the danger was in certain HAPPYTOT Stage 4 and HAPPYBABY Stage 1 and Stage 2 pouch meal products made by Nurture Inc., a New York based producer. These products could possibly have defects in their packaging which allows the pouches to swell or leak. Improperly sealed pouches, either swollen or leaking, could result in their contents being exposed to bacteria. Obviously, exposure to bacteria means that any children who eat this baby food might run the risk of food borne illness.
All of the meals being recalled are packaged in plastic pouches with plastic with plastic caps, and bear expiration dates between November 2010 and January 2011.
Products being recalled include:
• Green bean, pear & peas, NET WT. 4.22 OZ. (120g), UPC 8 52697 00127 9;
• Sweet potato, carrot, apple & cinnamon, NET WT. 4.22 OZ. (120g), UPC 8 52697 00128 6;
• Spinach, mango & pear, NET WT. 4.22 OZ. (120g), UPC 8 52697 00129 3;
• Butternut squash & apple, NET WT. 4.22 OZ. (120g), UPC 8 52697 00130 9;
• Banana, peach, coconut & prunes, NET WT. 4.22 OZ. (120g), UPC 8 52697 00131 6;
• Banana, peach & mango, NET WT. 4.22 OZ. (120g), UPC 8 52697 00132 3
• Mango, NET WT. 3.5 OZ. (99g), UPC 8 52697 00134 7
• Spinach Mango Pear, NET WT. 3.5 OZ. (99g), UPC 8 52697 00139 2
• Apricot Sweet Potato, NET WT. 3.5 OZ. (99g), UPC 8 52697 00136 1
Customers who purchased these products should contact Nurture Inc. this week for an exchange or refund. They can be called at 212-374-2779
Baby food recalls may seem even more dangerous and horrifying than other tainted food scares, since parents trust baby food makers to be particularly sensitive to the fact that their target consumers will be feeding them to very young children who have more delicate needs than adults, and who are less capable of understanding and communicating when they are seriously ill. Parents are often times more protective of their children than they are of themselves. This sort of event is not uncommon, though. Last fall saw a recall of Plum Organics baby food, and a failed attempt to initiate a recall on Gerber brand baby foods. It is not only the responsibility of parents to provide the best care they can for their children, but also the responsibility of the corporations that they trust to meet the high standards which society demands for care for children.
If you or someone you love has been injured as the result of a faulty defective product, it is important to talk to an experienced lawyer as soon as possible. Call (404) 531-9700 to schedule your free consultation at MLN Law.
Labels: child safety, consumer products, product liability, product recall
The government safety regulators have recalled all roll-up blinds and all Roman shades in homes with small children. The problem in this recall is the cords – these blinds all feature cords which a child can easily become trapped in and potentially be strangled to death.
Since 2001, there have been eight reported deaths and sixteen more near strangulations involving the cords of window coverings.Strangulation can occur when a child becomes trapped between the inner cords which control the binds, or when the cord becomes wrapped around the child’s neck. In the case of roll-up blinds, strangulation can occur when the child becomes tangled in the lifting loop. In both cases, the window coverings have exposed cords which pose the danger.
"Parents need to understand that these are hidden dangers, that a child can get entangled or strangled on these cords very quickly," said CPSC Chairman Inez Tenenbaum.
To illustrate the point, consider Collier Ursprung. The eighteen month old’s parents thought he was asleep in his crib, until the moment they heard a scream from his room.
"We scurried across the room to find him standing in his crib with the cord from the shade near his bed wrapped around his neck and he was unable to get out of it, and was struggling and tugging to get out of it," said Collier's father.
The boy’s father, Robert Ursprung, is a pediatrician. He managed to free his son and see to him immediately, and while the boy survived, it was very clear that the family had suffered from a close call.
Collier's mother, Susan Ursprung, will never forget the sight of the ligature marks the cord left in her son’s neck.
This is not the first time the CPSC has issued warnings and recalls about blinds. In fact, the organization has announced so many recalls that they are considering simply calling for a new mandatory redesign for children’s safety.
The CPSC recommends window coverings without cords for all homes with young children, or which young children regularly visit. It is impossible for parents to monitor their children constantly, and most parents do not realize just how quickly tragedies can happen. It only takes a few minutes for children to be seriously injured or killed.
In the short term, the CPSC advises that homes with these dangerous window coverings remove them, and keep them away from cribs or furniture which could serve to give young children access to cords. Special attention should be paid to keeping dangerous cords well out of reach.
Consumers who have Roman or roll-up shades in their homes should contact the Window Covering Safety Council immediately at www.windowcoverings.org or by calling (800) 506-4636 anytime to receive a free repair kit to make the window coverings safe.
For more information, visit the U.S. Consumer Product Safety Commission’s Web site.
Labels: consumer products, product liability, product recall
But that month, Zeppetella would be shot during a routine traffic stop. A gang member with a stolen hand gun shot him in the chest as he approached the window, severing an artery in his chest. Zeppetella was able to return fire, but lost his life as a result of his injury.
This story is saddening, but certain details change the tone from unfortunate but a hazard of his job to horrifyingly reprehensible. First, there is the fact that Zeppetella was wearing a bulletproof vest at the time. And second, there is that the vest’s manufacturer, Second Chance Body Armor, had known for years that their products were defective, and had taken no action to warn or protect their consumers.
As early as 1998, executives at Second Chance Body Armor knew that the Zylon material they used in their vest was prone to degradation which could render the supposedly durable armor penetrable. The Zylon, which was supposed to be strong enough to stop a bullet, was known to be untrustworthy.
In a memo written in 2001, one Second Chance executive recommended that the company take immediate action to notify their customers of the degradation problems with the vest – a memo written not only before Zeppetella died, but before his defective vest was even manufactured. In this memo, he argued that “lives and our credibility are at stake.”
However by the next year, no action had yet been taken, and in another memo company president, Richard Davis outlined potential courses of action as he saw them. This outline included, “operating as though nothing is wrong until one of our customers is killed or wounded.” This “option,” as Second Chance put it, guaranteed that someone would injured, potentially fatally, eventually.
Second Chance did not warn its customers until September of 2003, when they recalled some 130,000 of their bulletproof vests. This number did not represent all of their Zylon products on the market, and in 2005 they recalled another 98,000. They company argued that they could simply not afford to replace all of their Zylon products, leaving many still in circulation. One has to wonder if at how Second Chance executives valued the lives of the young men and women who relied on their vests for protection as they protected and served.
In the years between learning of Zylon’s deficiencies and the recall of the Zylon body armor, hundreds of thousands of Second Chance Body Armor’s vests were sold both to law enforcement officers and military personnel. They were even worn by former president George W. Bush.
If you or someone you know has been injured because of a bad product, it is essential to find a skilled attorney and protect your own health and rights as soon as possible. Contact an experienced Atlanta personal injury attorney. Call MLN Law at 404-531-9700 and schedule a free consultation.
Labels: consumer products, product liability, product recall
How could they have seen this tragedy coming? Because even before the FDA approved Ortho Evra, Johnson & Johnson knew that the patch’s method of delivering hormones to the bloodstream was giving women a much higher dose of estrogen than low dose birth control pills do.
Estrogen, as many people know, is the primary female sex hormone. Many women take estrogen supplements both as a form of oral contraception – often paired with progesterone – or in hormone replacement therapies. What fewer people know is that higher levels of estrogen increase the likelihood of blood clots and stroke, even in healthy women.
Over the past several years a growing body of evidence has connected female hormonal birth control to these increased risks of heart attack and stroke. These risks are higher in women over thirty-five, smokers, and those with other cardiovascular risks like high blood pressure.
Johnson & Johnson knew all this, and new from their own research that Ortho Evra carried too high of a risk for blood clots, and rather than halting its production, they hid the results. In fact, the company misreported their results by 40 percent.
The FDA were troubled when they reviewed the results of Johnson & Johnson’s clinical trials because there seemed to be troubling discrepancies in the research. However not knowing that the results had been willfully doctored to misrepresent the safety of the drug, they approved it for use in 2001.
Once Ortho Evra was on the market, Johnson & Johnson’s dishonesty only continued. The company avoided further research, including refusing to conduct comparison trials against the oral contraception, Ortho Cyclen. Internal memos sent within the company reveal that the reason for this refusal was “too high a chance that study may not produce a positive result for Evra” and fear that “risk that Ortho Evra may be the same or worse than Ortho Cyclen.”
Between 2002 and 2006, the FDA received reports of fifty deaths which were linked to the use of the Ortho Evra patch. Yet despite Johnson & Johnson having paid out over $68 million in settlements with hundreds of women who suffered from the increased averse side effects of this drug, Ortho Evra is still sold in the United States without even a black box warning.
If you or someone you know has been injured because of a bad product, it is essential to find a skilled attorney and protect your own health and rights as soon as possible. Contact an experienced Atlanta personal injury attorney, call MLN Law at 404-531-9700 and schedule a free consultation.
Labels: consumer products, product liability
However, the FDA lacks the resources to regularly inspect food plants. Typically, the organization will send inspectors to plants only every five or ten years. Between FDA inspections, state health inspectors do their best to pick up the responsibility of protecting consumers.
The Peanut Corp. of America (PCA), received acceptable marks on the 2006, 2007 and 2008 inspections of their Blakely, Georgia plant.
Yet in December of 2008, Shirley Almer, a seventy-two year old cancer survivor from Minnesota died of salmonella poisoning. The grandmother who had survived lung cancer and a brain tumor was killed by contaminated peanut butter.
Two months later, an Oregon three year old named Jacob Hurley began suffering from vomiting and bloody diarrhea. His pediatrician encouraged his parents to try to get him to eat again. The child’s parents tried to tempt him with his favorite food: Austin Toasty Crackers with Peanut Butter. Jacob did not recover, because without realizing it, his parents were feeding him more of the source of his problems. After being notified, the Oregon Office of Disease Prevention and Epidemiology tested the Austin Toasty Crackers with Peanut Butter, and found three out of six of the packets tainted with salmonella.
Jacob Hurley took eleven days to recover.
These two examples are among over 700 cases of salmonella, at least 9 of which proved fatal, which were traced back to contaminated peanuts from PCA’s Georgia plant. When investigators finally found the plant, they discovered unsanitary conditions, including cockroaches, leaky roofs, mold and machinery held together by duct tape. This plant, prior to its shut down, had processed 35 million pounds of peanuts a year.
The situation goes from tragic to horrifying, however. As investigations continued, the FDA found that PCA executives knew of the contamination. The PCA’s own internal testing had found the presence of salmonella on twelve separate occasions. Despite knowing this, PCA’s decision was to distribute the peanuts and approach another lab to conduct their internal health audits. This new lab gave plants a month’s advance warning of inspections, and awarded “superior” or excellent ratings to 98 percent of its clients.
Investigators later identified yet another problem plant, this one in Plainview, Texas. Conditions at the Texas plant included rodents and rodent excrement, as well as bird feathers found in a crawl space from which the ventilation system pulled air. Samples from this plant also tested positive for salmonella, and the PCA was forced to shut down this plant as well.
It may seem impossible and frightening that for two years, from 2006 to 2008, a company was able to distribute dangerously contaminated food – peanuts which ended up in numerous diverse products. Oscar Garrison, Georgia’s assistant agricultural commissioner, defended the state’s work, saying that it’s difficult for health inspectors to find problems when a company is determined to break the law.
Labels: consumer products, product liability, product recall
Consumers and businesses should expect to see more counterfeit bills, advised special agent Jeffery T. Gilbert.
“We cannot reiterate enough how important it is to look at your money,” said Gilbert. “Counterfeiting is a crime of opportunity. And it can be devastating on a business, a family, even our economy.”
Improving technology, particularly in the field of color copy machines, has made counterfeiting easier than ever for creative counterfeiters. By bleaching $5 bills and reprinting them as $100 bills, they are able to put their fake money on official US treasury paper. These fake bills on real paper are able to pass the counterfeit pen test.
There are many ways to tell if a bill is fake, even when it is printed on the correct paper. The Secret Service web site offers the following advice:
- The portrait on a genuine bill ought to stand out from the background, while that on a fake will appear lifeless or flat. Details in the back ground often seem too dark and lose distinction, merging together.
- The Federal Reserve and Treasury seals are clear and distinct on a real bill. On a fake bill, they may appear uneven, indistinct, or the saw-tooth points may seem broken.
- The borders on a counterfeit bill may seem blurred or indistinct. On a genuine bill, they should be clear and unbroken.
- A genuine bill has blue and red fibers woven into the paper throughout; they are embedded in the paper, not printed on the surface of it as in a counterfeit bill. Reproducing this distinctive paper is illegal.
- Serial numbers on a genuine bill are printed evenly spaced, in a distinct and consistent color and style. On fake bills, the numbers may vary, be too closely spaced, or otherwise differ from legitimately printed serial numbers. Serial numbers should be printed in the same ink as the Treasury seal.
- Suspect bills should be compared to a genuine bill of the same denomination to check for differences in portrait, serial number and vignette. Look for differences, not similarities.
- Bills of $500 denominations and above are no longer printed, and are being withdrawn from circulation.
Presently, the Secret Service is not seeing a localized spike in the Atlanta area, but given the risks, and the opportunity of consumers and staffs overwhelmed with the yearly holiday frenzy, there is still reason to be vigilant here. There is more than enough stress surrounding the holiday season without financial woes brought on by counterfeit money.
Labels: consumer products
Not everyone who has experienced this terrifying phenomenon has survived. 271 people died in accidents involving Firestone’s tires on Ford Explorers before their eventual 2000 recall. Many more, like Bailey, were seriously injured.
It was the largest tire recall in history.
Internal documentation eventually showed that both Ford and Firestone were well aware of the separation problem, and the rollovers that resulted from it, as early as 1997. Firestone had already received complaints from consumers who had purchased the Ford vehicle with their tires – a hundred times more complaints than they normally received for their products. The fact that there was a major problem with these tires was evident.
Later, Firestone employees would reveal that they punctured bubbles in the tire’s rubber to help disguise imperfections. Inspection and regulation of the finished tires was nonexistent.
At least three years after the company initially learned of the dangerous flaws in their product, in May of 2000, an investigation was finally opened by the National Highway Traffic Safety Administration. NHTSA’s concern was primarily over the issue of tread separation.
Tread separation occurs when the tread peels off the tire, often followed by the tire disintegrating. If this happened at speed, then it is likely to lead to a rollover. Vehicle rollovers are incredibly dangerous, and have a higher fatality rate than other kinds of accidents. Under normal circumstances, rollovers account for only about 3% of accidents, but 33% of fatalities – about a third of all fatalities. They are especially dangerous if drivers are not wearing their safety belts, but many drivers, like Donna Bailey, are seriously injured in rollovers despite proper safety belt use.
Under this attention, Firestone recalled 6.5 million tires. This would seem like a responsible move on the part of Firestone, finally, but the NHTSA warned the company of over a million tires with potentially worse faults than the recalled units. Firestone refused to expand the recall.
Firestone executives would go on to defend their decision against taking further action by saying, “We’ve got such a high volume of tires that looking for the root cause of the problem is like looking for a needle in a haystack.”
The NHTSA’s maximum fine of $925,000 was not enough to deter Firestone from inaction.
Donna Bailey sought justice through the civil court system, and was able to receive not only a monetary settlement, but also apologies from Firestone executives. Internal documents from Firestone were also released as part of the settlement.
If you have been injured in a car accident or due to a case of product liability, such as this one, then you need the services of a skilled attorney. If you have any questions, call MLN Law at 404-531-9700 to schedule a free consultation.
Labels: consumer products, product liability, product recall
In 2002, the medical manufacturer Guidant knew that their heart defibrillators were faulty. Due to a bad seal, fluid could penetrate the devices and cause short circuits. When the time came for the defibrillator to serve its purpose and deliver a shock to an irregularly beating heart, the Guidant defibrillator would do nothing.
Guidant new of this problem and corrected it, however, the companies executives also decided that it was most cost effective to continue to sell the defective devices which they still had in their inventory. 37,000 of these defibrillators were sold by Guidant after they were aware of the flaw and the product was redesigned.
It was not until 2005 that Guidant finally issued a warning about its product. Prior to that, the company’s executives made no effort to warn doctors or regulators of dangers with this device.
But what happened in 2005 which changed this? As is unfortunately often the case in situations where a device people rely on to protect their lives is untrustworthy: tragedy.
In the spring of 2005, Joshua Oukrop went for a bike ride with his girlfriend on the canyon trails near Moab, Utah. Joshua was 21 years old and enjoying his spring break, and he suffered from a genetic heart disease. He had taken steps to control his disease, among them having a Guidant defibrillator surgically implanted. His defibrillator failed to work when it was needed, and Joshua died.
In the months after Joshua Oukrop’s death, it became clear that it was not a one of a kind malfunction. Representatives from Guidant met with his doctor, Barry Maron, and revealed that they were aware of at least twenty-five other instances where the same model of defibrillator had short circuited. They insisted that the likelihood of the devices malfunctioning was small. The company argued that the risks of surgery to replace the defibrillators.
Dr. Maron notified the media, fearing that it would be only a matter of time before someone else died as a result of the company’s practices.
The ensuing investigations by the FDA and the media began to uncover just what Guidant knew of their products and when they knew it. In May 2005, The New York Times was preparing to print a front page article about how Guidant had neglected the health of their customers, and finally they began warning doctors of the dangers of the device. They still balked to admit that their defibrillators should be replaced.
After a 2006 inquiry by the Department of Justice, Guidant offered to cover the cost of replacement defibrillators, but declined to cover the cost of the surgery to replace them.
If you have been injured by a defective product contact an experienced Georgia personal injury lawyer. Call MLN Law at 404-531-9700 to schedule a free consultation.
Labels: consumer products, product liability
Georgia Representative Kevin Levitas will introduce the new food safety bill, which will call for felony punishment of one to 20 years for knowingly releasing contaminated food products that result in injury or death. The bill would also require companies to maintain better written records of food safety plans at processing plants.
“It sends out a strong message that Georgia stands for a high standard and we won't tolerate anybody who won't maintain those high standards. If you don't want to maintain them, then don't process food and don't grow it in the state of Georgia," said Rep. Levitas.
He plans to pre-file his bill at the state capitol. The Georgia General Assembly goes into session in January. While state legislation is being considered, some are still waiting for possible federal prosecution in the case.
"We certainly don't need to be spending state resources to duplicate what they're doing on the federal level. If the feds decide, hey we're not interested in doing this, that's the time for us to step in," Levitas said.
The federal government may indeed step in. Just last week the Atlanta Journal-Constitution reported that victims of the Salmonella outbreak are upset that there haven’t been any prosecutions yet, even thought FDA inspectors found roaches, mold, and a leaky roof.
Evidence shows that the head of the Peanut Corp. of America wrote emails to “turn them loose” after employees reported salmonella in the products. He wrote that his workers “desperately at least need to turn the raw peanuts on our floor into money.”
Still, federal prosecutors have not said whether or not Peanut Corp. of American executives will be facing charges.
“I thought prosecutions were a no-brainer,” said Lou Tousignant, whose father died from salmonella poisoning after eating contaminated peanut butter. “It seems like it’s been forgotten. That’s kind of how the country ebbs and flows. It’s in the news for a while, then everything quiets down.”
Creighton Magid, a products liability attorney in Washington, agreed with Tousignant: “It does surprise me.”
The victims are eager for action, reports AJC.
Gabrielle Meunier, whose 7-year-old son Christopher was hospitalized for a week after he was poisoned by salmonella, said, "The time is now. If the company's executives are spared prosecution, what does that say to the American public?"
GF “Pete” Peterman, the acting U.S. Attorney for the district including the peanut plant, did not comment to AJC reporters.
If the federal government does not take action, hopefully the state will take steps to ensure that food manufacturers will be properly punished for knowingly releasing tainted food to the public.
Have you been seriously injured by a contaminated or defective product? If so, contact an experienced Georgia personal injury lawyer as soon as possible. Call MLN Law at 404-531-9700 to schedule a free consultation.
Labels: consumer products, product liability
For a careful consumer, the internet provides a number of resources which can prove useful to understanding product risks. For example, The American Association for Justice provides a pamphlet which outlines a number of incidents where executives were well aware of the risks inherit in their products, and yet failed to act in any way to protect their customers.
Take the example of Propulsid, a prescription heartburn medication produced by Johnson & Johnson. Between 1993 and 1998, Johnson and Johnson made over a billion dollars on this product. By early 1995, it was already apparent that this drug was related to severe heart problems in some patients, and that it posed a particular risk to children. The Food and Drug Administration received growing numbers of reports of serious heart problems within the eighteen months hat followed. Federal regulators refused to clear the drug for pediatric sales – a warning which was not made public.
Johnson & Johnson agreed not to market Propulsid to children because of the increased chance of serious side effects, however they side stepped this agreement under the guise of educational efforts. These so-called educational efforts were, in fact, nothing more than a method of directing their dangerous product at the pediatric market. Ninety percent of the companies sales of cherry flavored Propulsid went to children, a fact of which documentation would show executives were well aware.
Lawsuits on behalf of injured patients would also show that Johnson & Johnson also avoided doing studies recommended by federal regulators, and that they suppressed the results of other studies which may have warned physicians of the dangers of their drug.
Gage Stevens was a three month old admitted to Pittsburg Children’s hospital with heartburn, diarrhea, frequent crying and vomiting. A specialist there saw him and recommended Propulsid for his condition. Gage died six months later of a heart arrhythmia. He was not alone. Before Johnson & Johnson finally removed Propulsid from the market in 2000, after two years of rejecting proposed changes to the product’s warnings and marketing, three hundred people had died of Propulsid. Sixteen thousand were injured.
Among one of the Johnson & Johnson’s executives’ notes was written, “Do we want to stand in front of the world and admit we were never able to prove efficiency!”
In 2000, the FDA was no longer able to ignore the consequences of Propulsid’s use. Rather than addressing the mounting safety concerns surrounding the drug, Johnson & Johnson announced that they would no longer be selling Propulsid.
If you or a loved one has been injured by any prescription drug, contact an experienced Atlanta personal injury attorney as soon as possible. Call MLN Law at 404-531-9700 to schedule a free consultation.
Labels: consumer products, product liability
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