Soft drink products that were previously recalled have now been classified by their risk level by the U.S. Food and Drug Administration (FDA). The FDA notices, posted on June 3, reveal that the drinks were produced by Charles Boggini Company and include the Pink Lemonade, Yellow Lemonade, and Yellow Lemonade X. While these products are not sold directly to consumers, they are distributed to other manufacturers and retailers.
According to the FDA’s enforcement report, one of the products, Yellow Lemonade X, falls under a Class III recall for “undeclared FD&C Yellow No. 5.” The Pink Lemonade and Yellow Lemonade fall under a Class II recall, with the Pink Lemonade being flagged for “undeclared FD&C Red No. 40” and the Yellow Lemonade containing “undeclared sulfites.” These undeclared ingredients pose potential risks to consumers.
FD&C Red No. 40, or E129, is a red food coloring that is used in various products. Some studies and health officials suggest that it can be linked to allergies, migraines, and mental disorders like ADHD. Similarly, FD&C Yellow No. 5 is a synthetic food dye found in soda and colored candy. Studies have shown that it may lead to allergic reactions or other adverse effects in individuals with asthma or aspirin intolerance.
To ensure consumer safety, the FDA requires that all color additives be clearly declared on product labels. This allows individuals to make informed choices regarding their consumption.
Sulfites, which are salts used as food preservatives, can also cause allergic reactions and other health issues in some individuals. The FDA mandates that food companies alert consumers to their presence when the concentration exceeds a certain amount.
The FDA documents indicate that all three recalls were voluntary and initiated by the company several months ago. However, on June 3, the FDA classified the recalls as a possible health hazard. The soft drink products were recalled across multiple states, including Arizona, California, Connecticut, Illinois, Missouri, Nevada, New Jersey, New York, and Pennsylvania.
Recalls are classified into three categories by the FDA based on the potential health consequences. A Class II recall means that the use of a violative product may cause temporary or medically reversible adverse health problems, with a small chance of major adverse events. A Class III recall indicates that the use of or exposure to a violative product is not likely to cause adverse health consequences.
In comparison, a Class I recall is the most serious form and is used when a product has a high likelihood of triggering a serious health problem or death. It is essential for consumers to be aware of these classifications to understand the severity of the issue.
The Charles Boggini Company has not issued a public statement regarding the recalls. The Epoch Times reached out to them for comment but did not receive a response.
In addition to the soft drink recalls, the FDA recently announced a Class III recall of about 1.9 million bottles of Fiji Water. Testing found the presence of a mineral and three types of bacteria in the recalled bottles. However, Fiji Water stated that there is no health or safety risk posed by these contaminants and that the affected bottles were mostly reclaimed. The company assured consumers of their commitment to safety and quality.
It is crucial for consumers to stay informed about product recalls and take necessary precautions to protect their health. By being aware of potential risks associated with undeclared ingredients or contaminants, individuals can make informed decisions about the products they consume.
