Hundreds of pounds of bubble gum sold in two states have been recalled after the Food and Drug Administration (FDA) classified the action as a Class II recall, according to federal records.
What To Know
According to FDA records, the recalled bubble gum was distributed in New Jersey and New York.
The recalling firm, Bader Enterprises Inc., is located at 115 27th Street, Brooklyn, New York.
Newsweek has contacted Bader Enterprises Inc. for comment via telephone outside regular business hours.
The recall involves Premium Food Bubble Gum packaged in 2.5‑ounce clear flexible plastic packaging and sold in unit cases totaling 30 pounds, according to FDA recall data.Â
The recall applies to all lots and codes of the product.
The FDA said the recall was initiated because the bubble gum contained undeclared colors, specifically FD&C Blue 1 Lake and FD&C Blue 2 Lake, which were not listed on the product’s labeling.Â
The total quantity affected by the recall is listed as 400 pounds.
The recall is identified by recall number H‑0539‑2026 and is tied to FDA Event ID 98398.Â
According to the FDA, the product’s lot number is 13. It has a best-by date of December 2028 and the Universal Product Code 015747199269.
The firm voluntarily initiated the recall, and the FDA’s records indicate that initial notifications to consignees or the public were conducted through multiple methods, including email, fax, letter, telephone or in‑person visits.Â
No news release was issued for the recall, according to the agency.
The FDA lists the recall as ongoing. It was initiated on January 16, and the agency assigned a risk classification on March 3.
No termination date has been provided.
What Is a Class II FDA Recall?
The FDA classified the bubble gum recall as Class II.
Under FDA definitions, a Class II recall involves a situation in which the use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is considered remote.
The FDA assigns recall classifications after evaluating the potential health risk associated with the reason for the recall and the information provided by the recalling firm.
Why ‘Undeclared Colors’ Could Be a Risk
The FDA requires certain ingredients, including color additives, to be properly declared on food labels so consumers can make informed decisions about the products they purchase or consume.
When colors such as FD&C Blue 1 Lake and FD&C Blue 2 Lake are not declared on a product’s label, consumers may be unaware of their presence.
The FDA flags undeclared ingredients because labeling accuracy is a key part of food safety and regulatory compliance.
The agency’s recall listing did not indicate whether any adverse reactions had been reported in connection with the bubble gum.Â
However, the FDA’s decision to classify the recall reflects its assessment of the potential risk associated with the labeling issue described in the recall record.
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