52USA Popping Boba with Passion Fruit Flavor contains unapproved food dyes (tartrazine, sunset yellow, allura red) that may cause allergic reactions. Recalled due to potential health risks from these additives.
Products contain unapproved colors, specifically tartrazine (FD&C Yellow 5), sunset yellow (FD&C Yellow 6), and allura red (FD&C Red 40).
The 52USA Popping Boba in Passion Fruit Flavor with a 7 lb net weight has been recalled because it contains unapproved food dyes. These dyes, including tartrazine, sunset yellow, and allura red, could cause allergic reactions in sensitive individuals.
The product contains unapproved food dyes that are not approved for use in food by the U.S. Food and Drug Administration. These dyes can cause allergic reactions in individuals sensitive to them, though the risk is generally low for most people.
People who purchased the 52USA Popping Boba in Passion Fruit Flavor from stores in the U.S. are affected. Those with allergies to the listed dyes are at higher risk.
Check for the 52USA brand Popping Boba with Passion Fruit Flavor. The product has a net weight of 7 lbs (3.2kg) and a shelf life of 18 months. It was distributed by Felicific Inc. in Queens, NY and has a UPC code starting with 8 1018 42125 1.
Look for the 52USA Popping Boba in Passion Fruit Flavor with a net weight of 7 lbs (3.2kg) and a shelf life of 18 months.
The product contains unapproved food dyes (tartrazine, sunset yellow, and allura red) that could cause allergic reactions in sensitive individuals.
The official recall notice does not specify a remedy or action steps for consumers.
The dyes are unapproved for use in food by the U.S. Food and Drug Administration and may cause allergic reactions in sensitive individuals.
We’ve drafted a message you can send 52USA to request your refund or repair — edit it as you like.
Subject: Recall H-0677-2026 — 52USA 52USA Hello, I own a 52USA that is covered by recall H-0677-2026 from 52USA. 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.
