Class IIOngoingVoluntary: Firm initiated
Pepsico Inc: food recall H-0009-2027
Pepsico Inc of Purchase, NY recalled 28 oz. Gatorade Lemon Lime, Gatorade Lemon Lime Zero, Gatorade Orange, and Gatorade Orange Zero. Reason: Undeclared Yellow No. 6 and/or Yellow No. 5. The FDA listed it as Class II in its Enforcement Report dated Oct 14, 2026; distribution: Alaska, Alabama, Arkansas, Arizona, California, Colorado, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Michigan, Minnesota, Missouri, Mississippi, North Carolina, North Dakota, Nebraska, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Utah, Washington, Wisconsin.
Record status as published: Ongoing. openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- 28 oz. Gatorade Lemon Lime, Gatorade Lemon Lime Zero, Gatorade Orange, and Gatorade Orange Zero.
- Product quantity
- 122,021 Cases (28 oz.)
- Reason for recall
- Undeclared Yellow No. 6 and/or Yellow No. 5
- Codes, lots and dates on the package
- Lot 091026 DL - JUN 07 27; Lot 091126 DL - JUN 08 27; Lot 072226 DT - APR 18 27; Lot 072426 TL - APR 20 27; Lot 073126 TL - APR 27 27; Lot 072926 TL - APR 25 27; Lot 073026 TL - APR 25 27; Lot 081026 TL - MAY 07 27; Lot 082126 OA - APR 18 27; Lot 080126 DL - APR 28 27; Lot 082026 DL - MAY 17 27; Lot 083126 DT - JUN 07 27; Lot 082526 KM - MAY 22 27; Lot 090426 KM - JUN 01 27; Lot 072726 TL - APR 23 27
- Distribution pattern
- AK, AL, AR, AZ, CA, CO, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MI, MN, MO, MS, NC, ND, NE, NJ, NM, NV, NY, OH, OK, PA, SC, SD, TN, TX, UT, WA, WI
- Recalling firm
- Pepsico Inc, Purchase, NY
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Sep 25, 2026 |
| Classified by the FDA | Oct 2, 2026 |
| Published in the Enforcement Report | Oct 14, 2026 |
Other recalls by Pepsico Inc
- H-0010-2026 · Oct 8, 2025 · Class II — Undeclared sugar in finished product-primary package does not reflect the product inside bottle.
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0009-2027 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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