Soft drink products produced by Charles Boggini Company have recently been classified by the U.S. Food and Drug Administration (FDA) according to their risk level. The FDA’s enforcement report reveals that the Pink Lemonade and Yellow Lemonade fall under a Class II recall, while the Yellow Lemonade X falls under a Class III recall. The Pink Lemonade was flagged for “undeclared FD&C Red No. 40,” the Yellow Lemonade for “undeclared sulfites,” and the Yellow Lemonade X for “undeclared FD&C Yellow No. 5.” These undeclared ingredients can potentially cause allergic reactions and health issues in some individuals.
FD&C Red No. 40, also known as E129, is a red food coloring commonly used in various products. Studies have suggested a potential link between this dye and allergies, migraines, and mental disorders like ADHD. Similarly, FD&C Yellow No. 5 is a synthetic food dye found in soda, colored candy, and other food items. Research has indicated that it may lead to allergic reactions or other adverse effects in individuals with asthma or aspirin intolerance.
The FDA mandates that all color additives be declared on product labels to ensure transparency and protect consumers. However, the Charles Boggini Company failed to declare these ingredients on their soft drink products, leading to the recalls.
Furthermore, the FDA requires that food companies inform consumers about the presence of sulfites when their concentration exceeds a certain amount. Sulfites, which are salts used as preservatives, have been linked to allergic skin reactions, digestive problems, stomach pain, and respiratory issues.
It is worth noting that all three recalls were voluntary and initiated by the Charles Boggini Company several months ago. The FDA classified them as possible health hazards on June 3, underscoring the seriousness of the situation.
The impacted soft drink products were distributed to various manufacturers and retailers across several states, including Arizona, California, Connecticut, Illinois, Missouri, Nevada, New Jersey, New York, and Pennsylvania. While a Class II recall indicates that the use of a violative product may cause temporary adverse health problems, a Class III recall suggests that the use or exposure to a violative product is unlikely to cause adverse health consequences.
The Epoch Times reached out to the Charles Boggini Company for comment but has not received a public statement from them regarding the recalls.
In addition to the soft drink recalls, the FDA recently announced a Class III recall of approximately 1.9 million bottles of Fiji Water. The recall was initiated due to the presence of a mineral and three types of bacteria in the tested samples. Fiji Water assured consumers that the recalled lots pose no health or safety risk. The company stated that the affected products were sold through only one distributor, and the majority of the recalled bottles were reclaimed with the remaining ones stored in warehouses for return. Fiji Water emphasized its commitment to ensuring the safety and quality of their products.
It is essential for consumers to stay informed about product recalls and take necessary precautions to protect their health. Checking product labels for declared ingredients and being aware of potential allergens or additives is crucial. Additionally, reporting any adverse reactions or concerns to the FDA can contribute to maintaining consumer safety and holding companies accountable for their product quality.
