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Recalls Watch

FDA recall 99991: Pepsico Inc: 28 oz. Gatorade Lemon Lime

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FDARecall 99991Food

What to do

The FDA record of this recall has no instruction for consumers. Compare the lot codes below with your product. If they match, do not use it, and follow the notice of the firm or ask the store where you bought it. Note from Recalls Watch, not agency text.

Read the official notice on accessdata.fda.gov (opens in a new tab)

Hazard

Why it was recalled

Undeclared Yellow No. 6 and/or Yellow No. 5
Text from FDA, unedited.

FDA classification: Class II. Use may cause temporary or medically reversible health consequences, or the chance of serious consequences is remote. Status: Ongoing.

Is it yours? Products and codes

Type the lot, batch, date code or model number printed on the product. It is compared here, in your browser, with the codes this notice lists. The code is also added to the page address (?lot=…), so a copied link or result carries it.

General information on recalls from the agency: U.S. Food and Drug Administration (opens in a new tab).

  • 28 oz. Gatorade Lemon Lime, Gatorade Lemon Lime Zero, Gatorade Orange, and Gatorade Orange Zero.

    Lot or code
    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
    FDA recall number
    H-0009-2027
    Quantity
    122,021 Cases (28 oz.)

Distribution (FDA): 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

About this record

Issued by
U.S. Food and Drug Administration
Firm
Pepsico Inc
Title
Composed by Recalls Watch from fields of the record; FDA records have no title.

If someone was hurt or swallowed something: call 911, or Poison Help at 1-800-222-1222.

About this recall

What is the hazard?

FDA states: “Undeclared Yellow No. 6 and/or Yellow No. 5”

What should I do if I have this product?

The FDA record of this recall has no instruction for consumers. Compare the lot codes on the notice with your product and follow the notice of the firm. The official report is linked on this page.

How do I know if my product is included?

Compare the lot or code printed on your product with the codes FDA lists on this notice, product by product.

How does the code check on this page work?

You type the lot, batch, date code or model number from your package and the page compares it, in your browser, with the codes FDA lists on this notice. It reports a match, a possible match (your code is part of a longer listed code) or no match. It only compares text: a notice that describes products by dates, sizes or “all lots” cannot be compared, so “no match” does not clear a product. The comparison runs in your browser and the page does not send the code anywhere, but the code is added to the page address (?lot=…): a link you copy, share or bookmark carries it, and whoever opens that link requests that address from this site.

When was this recall published?

FDA published recall 99991 on October 14, 2026.

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