PepsiCo Recalled 122,021 Cases of Gatorade
The products were recalled because they contain undeclared food dyes that may pose risks for certain consumers.
Updated on Oct. 5, 2026 in Nutrition

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PepsiCo has initiated a voluntary recall of 122,021 cases of Gatorade sports drinks distributed across 37 states. The recall was prompted by the presence of undeclared Yellow No. 5 or Yellow No. 6 dyes in the beverages.
Why it matters
Labeling requirements exist to protect consumers with specific sensitivities or allergies to artificial dyes from unintended exposure. The FDA has classified this action as a Class II recall, indicating a situation where use of the product may cause temporary or medically reversible adverse health consequences.
The FDA classified the voluntary recall of 122,021 cases of 28 oz. Gatorade bottles as a Class II action following the discovery of undeclared Yellow No. 5 or Yellow No. 6 dyes. The full scope of the affected lot codes remains under investigation to ensure all impacted units are identified.
The players
PepsiCo
A global food and beverage corporation based in Purchase, New York, that produces the Gatorade line of sports drinks.
FDA
The federal agency responsible for protecting public health by ensuring the safety and proper labeling of food and medical products.
The details
The recall involves specific 28 oz. bottles of Lemon Lime, Lemon Lime Zero, Orange, and Orange Zero flavors. Because these artificial color additives were omitted from the ingredient labels, consumers who are sensitive to these specific dyes may inadvertently consume them. To verify if a product is affected, customers should check the lot codes printed on the bottom or side of their bottles against the manufacturer's guidance.
Timeline
September 25, 2026: PepsiCo voluntarily initiated the product recall.
October 2, 2026: The FDA officially classified the action as a Class II recall.
October 5, 2026: News of the recall was published.
Health Landscape
This recall underscores the critical importance of accurate food labeling as mandated by the Food Allergen Labeling and Consumer Protection Act. The action serves as a safeguard to ensure that consumer-packaged goods meet the transparency standards required for public safety.
If you have purchased 28 oz. Gatorade bottles in the affected flavors, check the lot codes on the packaging to determine if your product is included in this recall. If you suspect an adverse reaction or have concerns about artificial dye sensitivities, discuss your symptoms with your physician.
The takeaway
Product recalls ensure that hidden ingredients do not pose unexpected health risks to the public. Always keep your packaging until you have verified it is not part of an active recall, and report any unexplained adverse symptoms to your primary care provider.
Further reading
For broader context on how to interpret nutrition labels and manage dietary restrictions, see our guide to Nutrition.
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