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Victims of Lead Poisoning: Examination of WanaBana Applesauce Scandal

Earlier this month, we witnessed a nationwide recall by the U.S. Food and Drug Administration (FDA), focusing on numerous brands of apple cinnamon pouches due to alarmingly high concentrations of lead found in them. Reports emerged from the North Carolina Departments of Health and Human Services and Agriculture and Consumer Services that four children had blood lead levels higher than usual. This was a potentially clear sign of acute lead toxicity. The children reported symptoms included headache, feelings of nausea, bouts of vomiting, diarrhea incidents, alterations in activity levels, and signs of anemia.

The brands WanaBana apple Cinnamon fruit puree pouches, Schnuck, and Weis Cinnamon applesauce pouches were distributed nationwide in retail outlets and online from multiple lots. All parents need to refrain from purchasing, consuming, or feeding these pouches to their children to avoid acute toxicity and additional symptoms like muscle aches, etc.

FDA’s Leading Hypothesis – Lead Exposure

A tainted FDA sample was mentioned on November 3, 2023, as part of an investigation into the elevated lead levels. After the Department of Agriculture & Consumer Services (NCDHHS) analyzed multiple lots, the case was transferred to the FDA’s Coordinated Outbreak Response & Evaluation (CORE) Network for further action. This is done with the Centers for Disease Control and Prevention (CDC) and local and state partners. As the recall impacts markets, our lawyers are looking at California test samples and customer information to try and protect public health. We will do our job if we can save at least one child!

Wanabana Apple Cinnamon Fruit and Weis Cinnamon Applesauce Pouches

Lead-contaminated applesauce has sickened numerous children in multiple states. State agencies, such as the Food and Drug Administration, detect high lead concentrations. So, it’s essential to highlight the role of legal support in such troubling scenarios.

Remember, most kids have zero obvious immediate symptoms, so listen to your lawyer and get checked out. Michael Ehline and the Ehline Law Firm stand ready to deliver legal assistance to victims of such negligence and misconduct in product liability cases.

After reading this, you will probably start seeing the FDA and CDC as political lapdogs, as opposed to really caring about public health. Through the example of this harrowing tale about lead poisoning resulting from harmless-looking applesauce pouches, we explain how Ehline Law Firm can guide and support the victims and their families. 

“We have a lead-poisoned child. But you’re perpetually waiting for that next shoe to fall,” Ricky said. “So we know right now he has a speech delay. But what does the future hold for him? We don’t know.”

Ricky’s quote from the affected parent unfolds the distress these families deal with. As the uncertainty about the future of their child shadows their everyday life, you have to understand your legal rights to justice in a toxic blood lead level case. Herein, we expand on the profound impact of such product liability cases and how Michael Ehline and Ehline Law Firm can assist you.

The foundation of a product liability case is that a product has been released in the market without adhering to strict safety standards and possibly causing harm to consumers. Any resulting harm directly attributed to the consumption or usage of this product can potentially be legal grounds for a product liability case. In such instances, it is of utmost importance to consult with an experienced law firm like Ehline Law Firm, spearheaded by attorney Michael Ehline, who specializes in handling these cases. 

The Importance of Legal Representation in Product Liability Cases 

The Centers for Disease Control and Prevention have issued an urgent alert to doctors across the United States, asking them to be vigilant for potential cases of lead poisoning among children. This comes in response to at least 22 toddlers with elevated blood lead levels, scattered across 14 different states, falling ill due to ingesting cinnamon apple puree and applesauce products in tainted applesauce pouches.

If you purchased WanaBana brand apple cinnamon fruit puree, Schnucks, or Weis brand cinnamon applesauce pouches, ruling out lead toxicity should be your top priority. Understanding the legal landscape surrounding the recalled pouches is not an easy task. Having experienced legal representation in these cases can prove decisive in a potential acute lead toxicity claim. 

“Legal representation can help you navigate the complexities, gathering sufficient evidence, and arguing your case effectively to make sure the erring parties are held accountable, ” says Michael Ehline of Ehline Law Firm.

Further, a well-established law firm, like Ehline Law, brings in a wide network of resources, such as medical experts, investigators, and other professionals, to build a robust case. 

How Michael Ehline and Ehline Law Firm Can Help Victims of Lead Poisoning 

The legal landscape becomes even more complicated when it comes to cases like the recent lead-tainted applesauce incident, where multiple families across several states could be affected. 

  • Meticulous investigation: Ehline Law Firm collects information regarding the offending product, its manufacturer, and its overall impact on the client’s health and life.
  • Interstate lawsuits: Given the scope of such a case, there might be an aspect of dealing with companies based in different states or countries. Ehline Law Firm is well-versed in handling complex interstate lawsuits.
  • Damages: Besides identifying the responsible parties, Ehline Law Firm also excels in determining and demanding rightful compensation for their clients. This includes immediate medical expenses and focuses on future medical costs, loss of income, pain and suffering, and other relevant damages.

With these aspects considered, it’s imperative to understand that a committed legal partner’s role is crucial in product liability cases. If you or a loved one has suffered due to a faulty product, don’t hesitate to reach out to Michael Ehline and Ehline Law Firm for legal advice and representation.

Lead Poisoning Statistics?

Following the above context, let’s delve deeper into the staggering data surrounding lead poisoning. The statistics are both alarming and serve as a stark reminder of the significance of this public health issue. 

Underestimating the Prevalence 

Lead poisoning, unfortunately, is far more prevalent than most people realize. The lead-contaminated apple puree pouches recently linked to dozens of cases is but the tip of the iceberg. These incidents have exposed the regulatory shortcomings and limitations in ensuring that food products for infants and young children are entirely safe. 

Yet, remarkably, many instances of lead exposure from food and other sources go unnoticed. This is partly because the symptoms are non-specific and can be misinterpreted for other issues. Unfortunately, this leads to an underestimation of the true number of lead poisoning cases. 

An Inordinate Risk for Children 

Children are especially at risk from lead exposure. This is primarily rooted in their developmental stage, with their bodies being susceptible to toxins and their consumption habits, which often include frequent hand-to-mouth activity. Furthermore, their small body size relative to the consumption of tainted substances could lead to an increased absorption of toxins. 

The Centers for Disease Control and Prevention (CDC) considers blood lead levels of 3.5 micrograms per deciliter or higher significantly elevated. Alarmingly, the children who consumed the lead-contaminated apple purees had blood lead levels ranging from 4 to 29 micrograms per deciliter. 

Long-Term Consequences 

The effects of lead poisoning are far-reaching and can have lifelong ramifications. It interferes with a child’s neurological development, potentially leading to reduced intellectual capacity, speech and hearing difficulties, and behavioral problems. 

These public health concerns underscore the imperative to address this grave issue proactively and protect our children from the hazards of lead poisoning. 

How did the lead end up in the supply of the applesauce pouches?

conducted to lead exposure to determine the exact cause of damage to the lead brain’s presence and in the nervous system, the applesauce slowed pouch growth and further contamination.

a significant problem that requires solutions at various levels. The FDA needs to establish protective standards to prevent such contamination. Food manufacturers should also thoroughly test their ingredients and finished products to ensure they are toxic metals-free.

Additionally, parents should stay informed and make choices that help reduce their children’s exposure to these harmful substances. The investigation into the lead contamination in the applesauce pouches is ongoing, and it is crucial to await the final results and recommendations from the FDA.

What actions has the FDA taken in response to the lead poisoning cases?

The FDA has taken several actions in response to the lead poisoning cases associated with the WanaBana apple cinnamon fruit purée pouches. On October 30, WanaBana recalled all the products, and on November 9, several lots made by the company but sold under different brand names were also identified. The FDA has issued a statement advising parents not to buy the product while they investigate the lead poisonings. They have also been screening incoming shipments of cinnamon from multiple countries for lead contamination, as cinnamon is believed to be the likely source of the contamination.

The FDA has emphasized the importance of regulatory action if specific products are unsafe. Additionally, the agency has made efforts to ensure that the recalled product is removed from store shelves and destroyed according to FDA guidelines. The FDA has acknowledged that the recalled WanaBana apple cinnamon fruit purée pouches were still on shelves at several Dollar Tree stores in multiple states.

In response, Dollar Tree has stated that it is working with store operations teams to ensure that the recalled product is no longer in stores and is destroyed according to FDA guidelines. The stores’ registers have also been programmed to prevent sales of the recalled product. The FDA’s response to the lead poisoning cases associated with the WanaBana apple cinnamon fruit purée pouches highlights the agency’s ongoing struggles in regulating baby food.

The FDA has faced scrutiny due to recalls of powdered baby formulas and the presence of heavy metals in commercial baby food. To protect babies from heavy metals, the FDA has drafted industry guidelines to minimize harm to children, which will be finalized by early 2025. The agency has also stated that it can take regulatory action even without new guidelines if it deems specific products unsafe.

What are some previous instances of baby food recalls and contamination?

One previous instance of baby food recall and contamination occurred last year when specific powdered baby formulas were recalled after three babies fell severely ill and one died from a bacterial infection. This recall exacerbated an ongoing formula shortage that began during the early days of the COVID-19 pandemic and left many parents struggling to feed their children. The government had to airlift millions of pounds of formula from overseas to address the shortage.

In 2021, a congressional investigation revealed that commercial baby food was tainted with significant arsenic, lead, cadmium, and mercury levels. This prompted the FDA to draft industry guidelines to minimize harm to children. The FDA spokesperson mentioned in the article stated that they expect to finalize these guidelines by early 2025.

However, even without the new guidelines, the FDA can take regulatory action if it deems specific products unsafe. In a 2019 report by Healthy Babies Bright Futures, a nonprofit focused on reducing babies’ exposure to harmful chemicals, it was found that 95% of baby foods tested contained heavy metals. This highlights the widespread issue of heavy metal contamination in baby food products.

The report emphasized the need for the government to take action to protect infants from these harmful substances and for food manufacturers to test their products for heavy metal content. These instances of baby food recall and contamination demonstrate the ongoing challenges faced by the FDA in regulating baby food and ensuring its safety. The recalls highlight the need for stricter standards, increased testing, and better oversight of the baby food industry to protect the health and well-being of infants and young children. So long as we are detecting extremely high concentrations of lead, we have to keep kids away.

How can Michael Ehline and Ehline Law Firm assist victims of lead poisoning in this specific case?

Michael Ehline and Ehline Law Firm can assist victims of lead poisoning in this specific case by providing legal representation and advocacy. They can help victims navigate the complex legal process and ensure their rights are protected. Firstly, Michael Ehline and his firm can thoroughly investigate the WanaBana applesauce scandal to gather evidence and determine liability. This may involve reviewing the recall information, analyzing the FDA’s findings, and consulting with experts in product liability cases.

Secondly, Ehline Law Firm can help victims understand their legal options and pursue a lawsuit against WanaBana. They can assess the damages suffered by the victims, such as medical expenses, pain and suffering, and potential long-term effects of lead poisoning, and seek appropriate compensation. Additionally, Michael Ehline and his team can negotiate with the responsible parties, including WanaBana and potentially other entities involved in the supply chain, to reach a fair settlement for the victims.

Citations:

Defects Force Ford to Recall Brakes and Software

On Friday, Ford announced that it involved recalling several affected vehicles belonging to different models it sold. In the announcement, Ford confirmed placing more than 700,000 vehicles. (Source National Highway Traffic Safety Administration – NHTSA.) Contact your local Ford dealership for more details about where to take your car. To learn more about these and other Ford recalls and other trucks, keep on reading.

We have all heard stories about lemons with oil leaks or stormy rear brake linings from neighbors and service advisors at the local dealership or local TV news. Sometimes there are no exact matches to your particular problem.

In certain situations, your only choice is to bring the car to the dealership, hope for a free inspection, and hope the dealers will replace the defective part based on the data derived from their customers and crew. Below, Michael Ehline, Los Angeles car accident attorney, will discuss the latest Ford Motor recall.

The Reason Behind the Ford Motor Recall

Ford officials at the Ford Motor Company automaker have revealed the causes that have led them to tell Ford Dealerships to go ahead with the recall. The recalled vehicles may have issues involving a software bug or a faulty body part needing repair.

For the software bug, the officials have explained that the bug may cause the safe braking system to either respond unexpectedly or not work at all on the affected vehicles. As for the faulty body part, they hinted it might end up causing oil leakage. So unlike an erroneous transmission failure, the safety risk here is far more significant.

Here, safety issues presented by a brake defect are typically fatal, especially with larger trucks making contact with smaller cars or a crash with motorcycle accidents. The software bug in the vehicles can cause the braking system of the towed trailers to malfunction and cause issues while braking the affected vehicles.

According to the officials, the separator installed in the particular vehicles for oil may get cracked. If the oil separator gets broken, it can result in an oil leakage, which may lead to a fire in the engine. It can result in the entire vehicle catching fire and putting the lives of the driver and the passengers at significant risk.

Vehicles Recalled by Your Local Ford Dealership Free of Charge

Ford has announced that the total number of vehicles they recall is 737,287. Out of the total of Ford vehicles identified, 345,451 include Ford Bronco Sports and Ford Escape. The Ford Bronco Sports models being recalled are from 2021 and 2022. As for the Ford Escape models, they are from 2020 to 2022. These particular vehicles are said to have software bugs.

The remaining 391,836 vehicles include F-550, F-450, F350, F-250, Expedition, Lincoln Navigator, 2021-2022 F-150, and 2022 Maverick. These particular models are said to have problems with the oil separator.

The officials have announced that Ford vehicle owners can check Ford’s website to see whether their vehicle is on the recall list. They have dedicated a particular team at Ford who will be closely looking into the matter and answering any of the vehicle owners’ queries.

How We Came To Know About the Ford Vehicle Recall Issues?

In the past couple of years, many small-level cases were raised regarding the malfunctioning of the software system and the oil leakage. Recently, the occurrences have intensified, and so has the damage caused due to these issues.

So far, Ford has been made aware of 8 cases surrounding the oil separator that caused the entire vehicle to get burned. Fortunately, none of the incidents resulted in crashes, injuries, or casualties.

Regarding the software bug, 67 cases have been reported to Ford regarding the software braking system for towed trailers. Once again, the incidents resulted in significant crashes or injuries.

Ford is to Start their Communications on the 18th of April

Starting 18th of April, Ford will have all the vehicles checked and assessed to identify the ones with potential faulty parts or software bugs. On the same day, Ford will launch its communication channel, where its representatives will call the vehicle owners to give an update.

They will confirm whether their vehicle has a body or software-related issue. If there is none, their car will be discharged with an attested inspection report.

Otherwise, the owners will be informed of the fault, and the Ford dealers will either fix the problem or replace the oil separator if needed. Similarly, the Ford dealers have been given the necessary training to carry out software fixing for the particular bug causing braking issues.

What About Potentially Defective Airbag Inflators?

This is not the first time Ford Vehicles Corporation has had to recall its vehicles. In the past few years, Ford has placed 775,000 and 620,000 cars on several occasions to address manufacturing faults. We previously discussed the problem with Takata Airbag inflators that caused quite a stir in the auto industry. In the past, Mazda and Ford tried to avoid recalling about 3 million vehicles with Takata airbag inflators that failed during crashes, including the vaunted Mercury Sable. And it’s not just the Ford Logo and a few Japanese cars. Even General Motors had airbag problems involving high heat and metal shrapnel harming vehicle occupants during a collision.

Takata utilized ammonium nitrate to ignite a tiny explosion to inflate airbags during a frontal collision. But the nitrate chemical mixture would deteriorate, fail to work, or ignite improperly, especially in desert areas, tropical, or extreme climate conditions over time, which the automakers had not disclosed.

Toyota recalled about 490,000 vehicles in Japan, China, Europe, and other locales. Eight automakers recalled more than 12 million U.S. vehicles for airbag inflators in that Japanese airbag inflator case where airbags exploded with excessive force.

This particular Ford recall notice comes on the heels of many defective seat belt claims and a faulty first gear, causing downshifting in some F-150s. Ford officials have recently undergone a slew of recalls from the Ford Focus, Ford Fiesta, Ford Explorer and Lincoln MKX, Lincoln MKZ, or Bronco Sport.

Oil Leaks Are Nothing Compared to This Auto Industry Bombshell?

We found other complaints on the NHTSA website that may interest Ford drivers or employees working at a Ford dealership. The key is to make the repairs before you or a loved one suffers a severe injury or a wrongful death.

Once that happens, customers will need the assistance of a highly experienced defective auto industry accident attorney near you. So get it in gear and request the owner or manufacturer of your vehicle fix these recalls immediately before the names of your vehicle occupants end up in the reports.

The law is clear; a recall notice does not clear a manufacturer from legal liability for your pain, suffering, lost wages, medical expenses, or other losses from a personal injury. But suppose you fail to get your car fixed with replacement parts when you are on notice of a defect or safety concerns. In that case, Ford Motor Co can use that as an excuse to blame you for part of the damages with federal regulators and any civil court suing them.

Under an identified recall, you don’t pay the cost to fix the problem, so pick up your phone, give the operator your vehicle identification number and handle it. Whether you live in Detroit or Los Angeles, it’s covered once reported!

Typically, you will receive your recall notice in a letter explaining the repair process and links to a website where the repairs would be covered.

Get a Free Consultation With a Ford Brake Defect Lawyer Today

Did you or your loved one suffer a severe injury or a wrongful death due to a broken software system or bad brakes? Ehline Law Firm offers free consultations to individuals seeking to recover an award of maximum compensation and justice. Our tier-one attorneys have assisted victims involved in accidents with SUVs and will cover the cost of your free case review.

You can schedule a consultation over the phone 24 hours per day, seven days per week, with a superior Los Angeles car accident lawyer. Don’t waste your energy with less qualified personal injury attorneys. The date you connect with us and form an attorney-client relationship, we will not stop fighting in your search for financial compensation and superior representations.

Feel free to dial (833) LETS-SUE 24/7 or use our helpful, confidential website. Contact us today for the best results and legal representation!

Does Aspartame Cause Cancer? Is It A Carcinogen?

I am Los Angeles personal injury attorney Michael Ehline. I am also a bodybuilder and amateur nutritionist. Below, I am going to discuss more what I suspected all along, that lab-created, nonnutritive sweeteners are bad for you! Americans always try to find quick solutions to control or lose excess body weight. Artificial sweeteners like Sodium Saccharine, Aspartame, and Splenda have long been the bane of fitness gurus and natural health advocates.

Your doctor may even recommend these to reduce the risk of diabetes, even though it may cause human cancer. We know that dogs, ants, and even cockroaches dislike Aspartame besides containing probable human carcinogens. Many argue that the American Cancer Society and government agencies are less scientific and more profit-oriented on the side of beverage makers. Many consumers have argued for years that the FDA and others needlessly mislead consumers about different substances in our foods and drinks.

Many food additive chemicals the FDA lets into our food are banned by scientific researchers for human consumption in Europe. The International Agency for Research on Cancer (IARC) (the cancer research arm of the World Health Organization (WHO)) will now classify Aspartame as “possibly carcinogenic to humans” for the first time. This artificial sweetener has been used in popular products such as Coca-Cola diet sodas (and other aspartame-containing beverages) and Mars’ Extra chewing gum since the 1980s.

What are Some Products Containing Aspartame?

Here are some store names commonly containing aspartame sweeteners:

  1. Equal
  2. NutraSweet (despite the fact there is no nutrition)
  3. Sweet’N Low
  4. Diet Coke (or any other diet soda brand)
  5. Crystal Light
  6. Trident gum (or other sugar-free gum brands)
  7. Sugar-free Jello or pudding
  8. Sugar-free candies or mints (various brands)
  9. Sugar-free yogurt or ice cream (various brands)
  10. Sugar-free protein bars or meal replacement shakes (various brands.).

This is not an exhaustive list. Also, aspartame-containing products can vary across different products and brands. We encourage consumers to check the ingredient list or consult the product packaging for more specific information.

The 2019 IARC Commission

In 2019, an advisory group comprising 29 scientists from 18 countries was highly prioritized for reviewing Aspartame by the International Agency for Research on Cancer (IARC) Monographs program. This program aims to evaluate the carcinogenicity of various substances and agents through a systematic and comprehensive assessment of available scientific evidence. The priority designation indicates that Aspartame underwent a thorough review by the IARC Monographs program between 2020 and 2024 to determine its potential carcinogenicity in humans.

The evaluation process involves critically analyzing and integrating relevant studies and data to reach a scientifically informed conclusion about the substance’s association with cancer. They say there is strong evidence that high doses of Aspartame are unnecessary to cause certain cancers.

It appears that the U.S. Department of Health and Human Services National Toxicology Program and the World Health Organization’s International Agency for Research on Cancer both used evidence-based approaches. But their report on carcinogens seems to differ over “human carcinogens” in most cases, including this reported controversy. Let’s go over the differences and similarities of the epidemiologic studies and findings of this chemical containing suspected carcinogens and whether the European Union epidemiologic studies should be re-evaluated.

First Observational Human Study on Aspartame?

This announcement comes in light of a first-of-its-kind observational study conducted in France, which included 100,000 adults and revealed a higher cancer risk among individuals who consumed more significant amounts of artificial sweeteners, including Aspartame. Finally, this artificial sweetener has been declared a possible potential carcinogen causing cancer among humans by the World Health Organization. AS REFERENCED IN THIS HEALTH STUDY, the WHO’s classification of Aspartame as a possible carcinogen indicates its potential role as a slightly higher cancer risk.

Although prior studies had limited evidence, there appears to be solid or sufficient evidence that high-intensity sweeteners known as Aspartame, like Diet Coke, are deadly, even at lower doses. For now, most studies favor the food sellers, and any risks of certain kinds of cancer appear to be outweighed by these low-sugar options in the U.S. anyways.

What Does the National Cancer Institute Say?

Before this European finding, I recently read “Artificial Sweeteners and Cancer,” as originally published by the National Cancer Institute. The NCI apparently disagree with IARC and WHO, asserting that THEIR available studies showed no evidence that these sweeteners cause cancer or harm in humans. So the issue seems to be the acceptable daily intake in humans instead of animal studies.

The Food and Drug Administration (FDA) also asserts that Aspartame is safe for the general population, provided it is produced following good manufacturing practices and used within approved conditions of use. Their conclusion is based on their research evaluations, often conducted on behalf of the food industry, assessing the safety of Aspartame and other food additives permitted as “artificial sweeteners.” (Source – FDA.)

What About the European Food Safety Authority?

The European Food Safety Authority (EFSA) is an independent agency of the European Union responsible for assessing and communicating risks associated with the food chain. It provides scientific advice and recommendations to ensure food safety and protect public health.

The EFSA evaluates a wide range of topics related to food, including additives, contaminants, genetically modified organisms, and pesticide residues. Its assessments are based on rigorous scientific methodologies and aim to inform policymakers, consumers, and stakeholders in making informed decisions regarding food safety in the European Union.

Cancer Risk With Human Carcinogens?

There is zero nutrition in these chemical mixtures. Aspartame, which is also used in some Snapple drinks, will be listed in July as “possibly carcinogenic to humans” for the first time by the International Agency for Research on Cancer (IARC), the World Health Organization’s (WHO) cancer research arm, the Reuters report said. The move is likely to pit the food industry against regulators. However, the FDA heads, many of whom work on pay later schemes in the industry, have for decades defended non-nutritive sweeteners. It appears the FDA and their food and beverage maker allies are already trying to minimize the severity of the European environmental health report.

What are Some Examples of Carcinogens?

Many substances and factors have been identified as definitive, probable, or possible human carcinogens. These include various chemicals, environmental pollutants, lifestyle factors, and exposures. It’s important to note that the classification of a substance as a carcinogen does not imply that exposure to it will always cause cancer but rather that there is scientific evidence suggesting a potential association with cancer development. The International Agency for Research on Cancer (IARC), a specialized agency of the World Health Organization (WHO), is responsible for evaluating the carcinogenicity of substances, including those contained in low-calorie sweeteners.

Examples of substances and factors that have been classified as carcinogens by the IARC include:

  1. Tobacco smoke, including both active and passive smoking
  2. Asbestos, a mineral fiber commonly used in construction materials
  3. Benzene, a chemical found in gasoline, emissions from industrial processes that can lead to occupational exposure to oxidized bitumens and other emissions, and even tobacco smoke
  4. Formaldehyde is a chemical used in various products, including building materials and household products
  5. Arsenic, a naturally occurring element present in certain minerals and used in various industrial applications
  6. Ultraviolet (U.V.) radiation from sunlight and tanning beds (known to cause skin cancer.)
  7. Certain types of ionizing radiation, such as X-rays and gamma rays
  8. Alcohol consumption
  9. Processed meat is associated with an increased risk of colorectal cancer.

These are just a few examples, and the list of identified carcinogens continues to evolve as new research emerges with humans instead of lab animals. It’s important to note that the classification of a substance as a carcinogen does not indicate its risk level. The level of risk depends on various factors, including the intensity and duration of exposure, individual susceptibility, and other contextual factors.

Formaldehyde and Cancer Risk

Aspartame, when metabolized by the body (heated in your body), can undergo a process called methanol metabolism, which involves the breakdown of Aspartame into its constituent components. One of these components is methanol, a small amount of which is released upon the digestion of Aspartame. In the human body, methanol can be further metabolized into formaldehyde. Formaldehyde is a naturally occurring substance in the body found in various foods and beverages.

The FDA and manufacturers assert that the conversion of methanol to formaldehyde from aspartame consumptiAspartamesidered to be within safe limits and does not pose a significant health risk. The FDA says the human body has natural mechanisms to process and eliminate formaldehyde, and the levels produced from the breakdown of aspartaAspartamenerally well-tolerated.

Can the Body Make Formaldehyde Without Aspartame?

The FDA points out that formaldehyde produced from aspartame metabolism is relatively tiny compared to the amounts produced from other dietary sources or even from endogenous metabolic processes in the body. The safety of aspartame artificial sweeteners has been extensively evaluated by regulatory agencies worldwide, such as the U.S. Food and Drug Administration (FDA), and it is considered safe for consumption when used within approved levels.

Other Concerns Raised by IARC

The IARC ruling, finalized earlier this month after meeting the group’s external experts, was intended to assess whether something is a potential hazard based on all the published evidence. However, it does not consider how much of a product a person can safely consume. This guidance for individuals originates from a distinct expert committee on food additives called JECFA (the Joint WHO and Food and Agriculture Organization’s Expert Committee on Food Additives), which is separate from the WHO. The report also incorporates findings from national regulatory bodies. Nevertheless, when the IARC issues comparable rulings for various substances, it often triggers consumer apprehensions and legal actions and prompts manufacturers to reformulate their products with alternative ingredients. Consequently, the IARC’s assessments have faced criticism for potentially confusing the general public.

The WHO Committee on Additives, JECFA, is currently reviewing the use of aspartame. The meeting commenced at the end of June, and its findings are scheduled to be announced on the same day as the public decision of the IARC, which is on July 14. Since 1981, JECFA has recommended consuming aspartame within the established daily limits. For instance, an adult weighing 60 kg (132 pounds) would need to consume between 12 and 36 cans of diet soda per day, depending on the amount of aspartame in the beverage, to potentially be at risk. This viewpoint has been widely endorsed by national regulatory bodies, including those in the United States and Europe.

An IARC spokesperson said the IARC and JECFA committees’ findings had been confidential until July. They added they were “complementary,” with IARC’s conclusion representing “the first fundamental step to understand carcinogenicity.” The additives committee “conducts risk assessment, and that determines the probability of a specific type of harm (e.g., cancer) that might occur under certain conditions and “levels of exposure.”

Food Industry v Regulators

The IARC’s rulings can have a considerable impact. In 2015, its committee concluded that glyphosate is “probably carcinogenic.” Years later, even as other bodies like the EFSA contested this assessment, companies still felt the decision’s effects. Germany’s Bayer 2021 lost its third appeal against U.S. court verdicts that awarded damages to customers blaming their cancers on using its glyphosate-based weed killers.

The IARC’s decisions have been criticized for being alarmist over hard-to-avoid substances or situations. It has previously been stated that working overnight and consuming red meat is in the “probably cancer-causing” class. It has also been said using mobile phones is “possibly cancer-causing,” similar to Aspartame. The FDA notes that the IRC is not a food safety body.

The FDA thinks this review of aspartame is not scientifically comprehensive. Critics say it is based heavily on “discredited research.” The secretary general of the International Sweeteners Association (ISA)) is not happy. The ISA body includes Mars Wrigley, a Coca-Cola unit. The secretary-general has “serious concerns with the IARC review, which may mislead consumers.”

French Study

Aspartame has undergone extensive studies over the years. A recent observational study in France involving 100,000 adults found that individuals who consumed more significant quantities of artificial sweeteners (sweetness chemicals), including aspartame, exhibited a slightly higher risk of cancer. It’s important to note that this study was observational in nature, meaning it can only establish a correlation and not a direct cause-effect relationship. Further research and studies on people who eat or drink these blended recipes are needed better to understand aspartame’s potential impact on cancer risk.

Italian Study

The Ramazzini Institute in Italy conducted a study in the early 2000s which suggested a link between aspartame and certain cancers in mice and rats. However, it should be noted that the first study could not establish a definitive cause-effect relationship between aspartame and increased cancer risk. The methodology of the second study has been questioned, including by the EFSA, which conducted its own assessment.

Aspartame has been authorized by regulatory bodies worldwide after thoroughly reviewing the available evidence, and significant food and beverage companies have defended its use for many years. The IARC’s decision to list aspartame as a possible carcinogen encourages further research to help draw more definitive conclusions for agencies, consumers, and manufacturers.

This development is likely to spark renewed debates on the role of the IARC and the overall safety of sweeteners. Recently, the WHO published guidelines advising against using non-sugar sweeteners for weight control, leading to discussions within the food industry, arguing that such sweeteners can benefit individuals looking to reduce their sugar intake.

Conclusion

Did we raise an eyebrow? Knowing what goes in your body should be a high priority to avoid disease exposure. We just discussed Aspartame, carcinogens, and cancer associated with this non-nutritive sweetener. This study and its findings have created a bad environment for those who manufacture and sell sweet chemicals. The International Council of Beverages Associations’ executive director Kate Loatman thinks we should be “deeply concerned” and warned it “could needlessly mislead consumers into consuming more sugar rather than choosing safe no- and low-sugar options,” without nutrient sources added. She likely fears false reports of cancer, lymphomas, or carcinogenesis in humans could harm her industry sales goals.

Her side argues that higher consumption of aspartame-containing beverages has not been associated with the development of lymphoma, leukemia, or brain cancer in following studies commissioned by her side after much analysis by the world’s top food and beverage-employed scientists. As the debate continues, fitness types will likely continue not using artificial sweeteners, and others probably won’t care or call for more regulation of food and medicine. Below are some references for members of the public and scientific communities who exposed health risks to men and women, whether they consumed larger amounts or not. If you need to speak with a personal injury lawyer in Los Angeles, call (213) 596-9642. We are ready to help people 24/7, 365 per year! You can also leave your follow up comments here.

Citations:

  • Lim U, Subar AF, Mouw T, et al. Consumption of aspartame-containing beverages and incidence of hematopoietic and brain malignancies. Cancer Epidemiology, Biomarkers, and Prevention 2006; 15(9):1654–1659. [PubMed Abstract]
  • National Cancer Institute. (n.d.). Artificial Sweeteners and Cancer Risk: Fact Sheet. Retrieved from https://www.cancer.gov/about-cancer/causes-prevention/risk/diet/artificial-sweeteners-fact-sheet
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Baby Talc, Johnson & Johnson & Legal Rights

Understanding The Causes Of The Johnson And Johnson Lawsuit

Word defect with magnifier and target. Concept of zero defects or tqm
Word defect with magnifier and target. Concept of zero defects or tqm.

The Johnson & Johnson lawsuit highlighted several significant aspects of product liability law and responsibility. The drug and personal care giant was recently targeted by other recent lawsuits over one particular concern. The products from the company led to cancer and the severe effects of this terrible disease. Besides, some evidence emerged that the corporate giant understood its product’s risks and what could have happened when consumers used their baby powder. This is a significant concern for the general public and a significant cause of a lack of corporate responsibility.

We run down the circumstances of the lawsuits and the product itself. Furthermore, our legal team examined some of the specifics regarding the case and what consumers can do. Again, the $100 million settlement is likely just the beginning. There are still legal options for families affected by the use of this product. Utilizing the precedent built by this case, there is an opportunity to right this terrible wrong.

Michael Ehline is a leading top-10 personal injury attorney based in Los Angeles. He and his team recovered millions for clients injured by defective products and accidents. He is specialized in cases such as products that lead to severe injury. He also studied the talcum powder cases since the beginning.

For more info or to speak with an attorney 24 / 7, call him at the number below or email him at losangeles@ehlinelaw.com. Read more about Ehline and the cases that his firm works on here.

What Was The Baby Powder/Talc Asbestos Lawsuit About?

The news of $100 million coming from Johnson & Johnson is excellent news. It is also something that we have been following since the beginning. Fortune reported on the recent settlement and its implications. Johnson & Johnson has been under fire for four years over talc in their baby powder and other products. Overall, Fortune reported that there had been about 20,000 total lawsuits regarding the products.

Furthermore, Johnson & Johnson also admitted some issues. This includes an October 2019 recall of 33,000 bottles of baby powder due to asbestos contamination. Moreover, the company made major changes regarding its products due to the concern over talc use. In May 2019, Johnson and Johnson decided to stop selling talc-based baby powder in the North American market.

While the company asserts its products are safe, it decided to yank the shelf’s power. Furthermore, the recent decision was the first time the company settled any cases regarding talc. This is likely a bellwether for future suits and settlements.

What Is The Risk Of Talc To You And Your Baby?

The many lawsuits regarding talc revolve around the elevated risk of cancer from using this product. In particular, this is caused by how the product is mined. In multiple cases, the talc that made it into consumer products was mixed with varying amounts of asbestos. Asbestos has long been known as a cancer-causing material. Furthermore, there have been breast and ovarian cancer cases linked to using talc powders.

What Did Johnson & Johnson Know?

Johnson & Johnson claimed that it saw no danger in using its products. However, a lengthy investigation shows that the pharma giant understood its products’ base material risk. Far from the generic denials from J&J, the internal memos tell a different story. As far back as 1971, the company knew of the concern over its talc supply. One company executive called for a new source of talc due to the risk of asbestos contamination. Furthermore, the issue was raised again in 1973– the New York Times cites his own words that the powder may include products that “might be classified as asbestos fiber.”

What Is The Risk Of Talc?

Talc, by itself, is harmless. There is a reason why the product is used in a number of health and personal services products. However, how it is mined makes all the difference. Companies like Johnson & Johnson used mines that also had asbestos traces in them. Asbestos is highly toxic and has a long history of causing cancer. Johnson & Johnson was well aware of the product’s concern, including using their influence to attack research showing that very fact. In one case cited by the New York Times, the company even forced the Food and Drug Administration not to release such findings.

The $100 million lawsuit also followed a much larger $4.69 billion case when 22 women with ovarian cancer sued J&J. This shows the severe risk of contamination due to talc with asbestos. Furthermore, the company sold the product potentially contaminated with asbestos for decades. The company may be on the hook for far more lawsuits and dollars than those already in court.

What Must I Do If I Was Affected By Johnson & Johnson Baby Powder?

If you or a loved one were contaminated and affected by using Johnson & Johnson or other bands of baby powder, you have legal rights. Our team at Ehline Law specializes in handling cases such as cancer caused by asbestos. This includes more traditional effects, including mesothelioma, and the impact of ovarian and breast cancer, possibly caused by using such products. Ehline Law listens to your story and helps design a battle plan to get you paid back by the people who harmed you.

Moreover, our service covers you every step of the way, including, in some cases, the medical costs of such treatment upfront on a medical lien basis. Because we have earned the trust of local medical professionals we have worked with over the years, we can leverage this for your direct benefit. That way, clients like you can get the most accurate diagnosis as a starting point.

Our negligence law professionals seek to make you whole through our expertise, contacts, and superb reputation. Furthermore, we will assist in any way possible and offer a free, no-pressure consultation anywhere in the state. We follow Coronavirus protocols to understand better where you are coming from and how we can best help your family. We are here for you in this difficult time. Contact us on our online form at (213) 596-9642 or losangeles@ehlinelaw.com.

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Honda Pilot and Passport Recall Information with Product Defect Lawyers

This Recall is affecting Two Major Vehicle Lines

When vehicles fail, it can lead to devastating accidents, millions in lawsuits against vehicle manufacturers, and a bad reputation. Unfortunately, Honda faced vehicle problems and had to make four separate recalls for specific models. Let’s review the Honda Pilot and Passport recall information with Ehline Law and our California product defect lawyers. Due to the factory issue, these vehicles may not have been properly constructed, leading to concern about a catastrophic failure during a collision.

Consumer Affairs reported on the issue; according to the Recall, the vehicles have severe structural integrity issues. The company said that the front frame left and right side upper members could not have been adequately welded to the car’s unibody. As a result, in case of a crash, there is a chance that this would not provide adequate protection case of a collision. This could lead to an increased event of severe injury or death.

Honda Recalled 1.6 Million Vehicles in 2020 after Problems Surfaced

In August 2020, Honda published critical information documents with the National Highway Traffic Safety Administration (NHTSA) and recalled a total of 1.6 million vehicles, including Odyssey minivans, pilot vehicles, and passport SUVs, in the United States after discovering several issues.

Let’s look at the recall details and why Honda decided to notify owners about the issues in their cars.

This affects the 2019 and 2020 Pilot models and the 2019 Passport line. Honda announced that it would notify owners of these vehicles after December 1, 2019. If you were involved in an accident due to this error, your priority is to contact an expert.

Find Out More About the Honda Recall

For more info on the Honda recall or your legal rights, contact the Ehline Law Firm APLC today. Our skilled attorneys have managed similar cases before, winning millions for our clients if they were injured due to a car company’s negligence.

Our team is second to none in the state of California and offers a variety of options, especially for crash victims. These consultations are free, and we don’t ask for a cent unless we collect for you. That is our promise.

Power Sliding Door

About 324,194 Honda Odyssey minivans (2018 to 2020 models) faced a slight problem with the power sliding doors. The company recalled the cars after discovering that water can freeze between the power sliding door and the outside door handle, which could restrict the door latches.

The defect on the 2019 and 2020 models of the Honda Odyssey could allow the water to seep into the backup camera, affecting the rear camera image.

Backup Camera

Specific models of the Honda Passport and Pilot SUVs faced faulty software programming resulting in issues with the backup camera during reverse. Honda decided to do a software update to address the problem.

Engine Oil Pressure

The Japanese public multinational conglomerate manufacturer recalled about 607,784 cars, including Odysseys (2018 to 2019 models), Honda Passports (2019 and 2020 models), and Honda Pilots (2019 to 2021 models), after they discovered a defect in the gauge cluster displays.

The unit’s display failed to show vehicle indicators such as engine oil pressure, speedometer, and gear selection.

Hood Latch Striker

The Japanese car manufacturer recalled about 750,000 Passport, Pilot, and Ridgeline vehicles after discovering a defective hood opening, which could cause the hood to fly open. The gap in the hood could allow air into it, causing an upward pressure, weakening the component that held onto the hood latch striker over time and causing the entire hood to open.

NHTSA Safety Honda Vehicle Recalls Summary

Here are some of the details for the recently recalled vehicles by Honda:

  • November 28, 2021 – Issues with the hood connection
  • March 24, 2021 – Issues with the fuel pump causing the engine to stall
  • March 10, 2021 – Issues with over-cured tires causing sudden air loss or belt edge separation, increasing the risk of an accident
  • July 27, 2020 – Issues with the rearview camera display and functioning instrument panel
  • February 5, 2020 – Certification label with weight load information not readable
  • October 30, 2019 – Issues with body welding on the front frame left and right side upper members.

For all the issues facing vehicles, the company announced that Honda dealers would fix all the problems free of charge. Vehicle defects can cause serious accidents. If you suffered injuries due to a vehicle defect, contact us at (833) LETS-SUE for a free consultation with our legal experts, as you may qualify for compensation.

Let us know if you would like more info on the Recall Recalldiscuss further. Please fill out the contact form on this site 24/7 and contact one of our legal experts today. We defend you and your family’s right to a complete physical, emotional, and financial recovery. Contact Ehline Law for more info.