Bader Enterprises recalls Premium Food Bubble Gum with undeclared blue dyes. All units sold in 30-count cases contain FD&C Blue 1 Lake and Blue :2 Lake. No remedy provided.
Contains undeclared colors (FD&C Blue 1 Lake and FD&C Blue 2 Lake).
Bader Enterprises is recalling all Premium Food Bubble Gum sold in 30-count cases due to undeclared food dyes. This poses a risk of allergic reactions for people sensitive to these dyes. Consumers should check their product for the specific lot numbers and stop using if they have the product.
The gum contains undeclared food dyes (FD&C Blue 1 Lake and FD&C 2 Lake) that can cause allergic reactions in sensitive individuals. These dyes are not listed on the product label, which may lead to unexpected allergic reactions.
People who purchased the Premium Food Bubble Gum in 30-count cases from stores. Those with allergies to FD&C Blue 1 Lake or Blue 2 Lake are most at risk.
Check for the 2.5 oz clear flexible plastic packaging and 30-count cases. Look for lot numbers with '13 BEST BY : DEC-2028' and UPC codes starting with 015747199269.
Look for lot numbers with '13 BEST BY : DEC-2028' and UPC codes starting with 015747199269.
The product contains undeclared dyes that may cause allergic reactions in sensitive individuals, so it is not safe for everyone.
Check for 2.5 oz clear flexible plastic packaging in 30-count cases with lot numbers '13 BEST BY : DEC-2028' and UPC codes starting with 015747199269.
The recall does not provide a remedy, so consumers should check their product and avoid using it if they have allergies to the dyes.
We’ve drafted a message you can send Bader Enterprises to request your refund or repair — edit it as you like.
Subject: Recall H-0539-2026 — Bader Enterprises Bader Enterprises Hello, I own a Bader Enterprises that is covered by recall H-0539-2026 from Bader Enterprises. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
