A group is charging soda makers with endangering the public’s health by including what they say is a cancer-causing chemical in their products.
The Center for Science in the Public Interest has petitioned the Food and Drug Administration to ban 4-methylimidazole from soda. The group has claimed that studies have shown unsafe levels of the chemical, which is used to provide caramel coloring in soft drinks, in such popular brands as Coca Cola and Pepsi.
Their findings, though, are divisive. The FDA has said that it would take more than a thousand cans of soda per day to reach the level of risk that the group is claiming. And the American Beverage Association has stated that the company is simply trying to use scare tactics to push their agenda.
But the CSPI persists, saying that they found 140 micrograms of the chemicals in a 12 ounce soda serving, higher than the 29 microgram limit suggested by the state of California. They say that translates to 5 out of 100,000 people that will contract cancer.
The FDA, for their part, places a cap on the caramel coloring at 250 parts per million.
As a personal injury lawyer in Long Beach, I find the battle over consumer safety to be of particular importance. No matter which way this petition goes, I’ll be keeping close tabs on the results. I feel that knowledge of FDA rulings is important to a Los Angeles personal injury lawyer.
According to news sources, U.S Marshals ended up seizing dietary supplements and drugs manufactured by Syntec Inc today, after The Food and Drug Administration said that the company allegedly used false claims in their advertisements in regards to the safety and effectiveness of their products.
The company, Syntec Inc, allegedly makes claims in its promotional materials concerning the ability of its products to cure, treat or prevent diseases such as cardiovascular disease, asthma, and glaucoma. These claims are not approved by the FDA, which has reportedly filed a complaint against the company.
The company has also reportedly failed to follow current good manufacturing practice (cGMP), which are requirements enforced under federal law. FDA investigators have also allegedly found various cGMP violations during previous inspections.
As a Riverside personal injury lawyer, I appreciate all efforts being made to ensure increased drug safety standards for everyone . I hope this information can help raise awareness about this product and keep consumers safe. If you or a loved one has been injured through the use or consumption of a defective product, speak with a personal injury attorney Riverside to learn about the legal options available to you.
According to news sources, the Food and Drug Administration has announced that a Chicago based ready-to-eat sandwich maker has shut down manufacturing after a repeated history of violations and a reported Listeria outbreak.
The company, Triple A Services Inc., has announced the closure of of the manufacturing facility after agreeing to stop producing and distributing its ready-to-eat sandwiches. The agreement also stipulates that the company hire a sanitation expert to oversee the company’s sanitation program and ensure its compliance with existing FDA safety regulations.
There have been no illnesses to date relating to the consumption of the company’s sandwich products.
The company’s manufacturing facility reportedly experienced a Listeria monocytogenes outbreak recently, helping prompt the decision to close the facility. Listeria can cause severe or even fatal infections to those with weak immune systems, the elderly and children.
As a Los Angeles personal injury lawyer, I urge you to be mindful of threats from food-borne bacteria. Consumers that have purchased a known defective product should stop using it immediately. If you or a loved one have been injured by a defective product, I urge you to contact a product liability lawyer Los Angeles to learn about your legal options.
According to news sources, The Food and Drug Administration is warning multiple surgical centers against using misleading advertisement to promote Gastric Band operations without stating the inherent risks involved.
The FDA is targeting a total of 8 surgical centers that perform the operations as well as a marketing firm in California for misleading consumers by not divulging into the serious risks associated with Lap-band operations in their advertisements. The FDA said that consumers unaware of the inherent risks could be influenced by the misleading advertisements
The serious risks involved in the surgical operation include but are not limited to:
- Stomach pain
- Strecgin of the stomach pouch
- Stretching in the esophagus
- The moving of the band, requiring additional surgery
- The erosion of the band within the stomach wall, requiring additional surgery
There are two gastric bands that have acquired the approval of the FDA and those are the Realize Adjustable Gastric Band as well as the Lap-Band.
As a Los Angeles personal injury attorney, I deeply appreciate the efforts being made by authorities to ensure smarter and more efficient safety practices to protect the general public. As a product liability lawyer Los Angeles, I hope that the conclusions of this research will lead to practices.
According to news sources, the Food and Drug Administration is taking a closer look at the arsenic levels found in juices and juice concentrates to ensure compliance with existing safety standards.
The FDA has been monitoring the levels of arsenic found in juices sold nationwide for more than 20 years and is currently taking additional steps to ensure the safety of the public’s health.
These steps include enhancing the existing surveillance of apple juices and concentrates to identify high levels of arsenic wherever they may be found. Results for about 90 samples of juices should be expected shortly. Testing samples of imported juice products from China is also currently underway. Lastly the FDA will work with the Environmental Protection Agency to ensure collaborative efforts geared towards reducing the overall levels of arsenic in juices and concentrates.
Arsenic exists in the environment as a naturally occurring substance. However, an intake of increased amounts of the substance can be highly toxic.
As a Los Angeles personal injury lawyer, I hope the conclusions of this research will lead to more effective safety measures to protect consumers. If you’ve consumed a contaminated product and are experiencing symptoms, I encourage you to seek medical attention. If you’ve been seriously injured by eating food product, I urge you to contact a Los Angeles product liability attorney to learn about your legal options.
According to news sources, the Food and Drug Administration has announced that they will be considering additional safety measures such as potentially ordering new warning labels for newer birth control drugs after ongoing research suggested that the newer drugs were more likely to cause blood clots than older birth control drugs.
The FDA will meet later in the week to explore the different safety measures it can take after research suggested that newer birth control drugs such as Bayer’s Yaz and Yasmine, may cause a slightly increased chance of blood clots.
The newer drugs have gained popularity since they appeared to reduce certain side effects found in older birth control drugs, such as mood swings and bloating. The newer drugs credit a certain version of a female hormone found in the drug for the decreased side effects.
Although the increased risk of blood clots associated with the newer drugs are slight, blood clots in themselves are extremely dangerous and can cause severe or even fatal injury.
As a product liability lawyer Los Angeles, I understand the severity of the hazards entailed in using defective products. I hope this information can help raise awareness about the product. If you or a loved one has been injured through the use of a defective product, speak with a personal injury lawyer Los Angeles to learn about the legal options available to you. Please, continue to visit our blog for regular updates about unsafe and dangerous consumer products.
