In case you are chewing one of these vibrantly coloured candies, as you read this article, throw it right away! The FDA has issued a recall of a popular brand of candy in 8 US states. Blooming Import Inc. in Brooklyn, New York, has initiated a voluntary recall of its Golden Crop Candy due to undeclared colour additives, including an unapproved dye. Here’s everything you need to know about the recall.
What is the recalled product?
The recalled product is Golden Crop Candy, packaged in 10-ounce containers, with a total of 74 cases affected. Each wrapped candy is about 283 g. The FDA has classified this as a Class II recall.
Why is the product recalled?
The firm initiated a voluntary recall on the candies as they contain undeclared colour additives - Blue 1, Red 40, and Acid Red 18. Not listing it on the label violates FDA regulations. While Blue 1 and Red 40 are permitted colours, Acid Red 18 is not. It is worth noting that the FDA has previously banned Red Dye No. 3, citing concerns over its links to cancer. Usage of Acid Red 18 has raised concerns about potential health risks, including hyperactivity in children. The FDA notes that reactions to color additives are rare but possible, particularly for those with sensitivities.
What is a Class II recall?
According to the FDA, a Class II recall is ‘a situation in which 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 remote.’ Recalls are classified into a numerical designation (I, II, or III) by the FDA to stress the relative degree of health hazard presented by the product being recalled.
How to identify the recalled products?
The affected Golden Crop Candy can be identified by looking at its packaging. Check the packaging for this code to confirm if your product is part of the recall.
The candy was distributed to retailers in the following states:
If you have the recalled candy, you should stop using the product and return or discard it. If you experience an adverse reaction, contact your local FDA Consumer Complaint Coordinator to report the issue.
What is the recalled product?
The recalled product is Golden Crop Candy, packaged in 10-ounce containers, with a total of 74 cases affected. Each wrapped candy is about 283 g. The FDA has classified this as a Class II recall.
Why is the product recalled?
The firm initiated a voluntary recall on the candies as they contain undeclared colour additives - Blue 1, Red 40, and Acid Red 18. Not listing it on the label violates FDA regulations. While Blue 1 and Red 40 are permitted colours, Acid Red 18 is not. It is worth noting that the FDA has previously banned Red Dye No. 3, citing concerns over its links to cancer. Usage of Acid Red 18 has raised concerns about potential health risks, including hyperactivity in children. The FDA notes that reactions to color additives are rare but possible, particularly for those with sensitivities.
What is a Class II recall?
According to the FDA, a Class II recall is ‘a situation in which 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 remote.’ Recalls are classified into a numerical designation (I, II, or III) by the FDA to stress the relative degree of health hazard presented by the product being recalled.
How to identify the recalled products?
The affected Golden Crop Candy can be identified by looking at its packaging. Check the packaging for this code to confirm if your product is part of the recall.
- Product Description: Golden Crop Candy (10 oz. (283g) wrapped candies)
- Code Information: UPC code: 73476513450.
- Product Quantity: 74 cases total
The candy was distributed to retailers in the following states:
- New York
- Pennsylvania
- Maryland
- New Jersey
- Massachusetts
- Missouri
- Delaware
- Texas
If you have the recalled candy, you should stop using the product and return or discard it. If you experience an adverse reaction, contact your local FDA Consumer Complaint Coordinator to report the issue.
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