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Lower risk Food recall · FDA · Published November 2, 2018

Frito-Lay Crunch & Pop Mix Variety Pack Sack Recall: Undeclared Milk in Popcorn

Frito-Lay recalls 16-count Crunch & Pop Mix Variety Packs with potential undeclared milk due to cheese-flavored chips. Consumers should check for specific use-by dates and manufacturing codes.

🇺🇸 FDA recall #F-0690-2019FoodFrito-Lay ›
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Recalling firmFrito-Lay, Inc.7701 Legacy Dr · Plano, TX 75024-4099
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What happened, in plain English

Frito-Lay is recalling 16-count Crunch & Pop Mix Variety Packs that may contain cheese-flavored chips with undeclared milk. This poses a risk for people with dairy allergies who might consume the popcorn without knowing. Read more at govinfonow.com/recall/18097-frito-lay-crunch-pop-mix-variety-pack-sack-recall-undeclared.

Source Summary by GovInfoNow · govinfonow.com/recall/18097-frito-lay-crunch-pop-mix-variety-pack-sack-recall-undeclared · Updated October 5, 2026 · FDA enforcement record: FDA #F-0690-2019

Cite this page

“Frito-Lay Crunch & Pop Mix Variety Pack Sack Recall: Undeclared Milk in Popcorn.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/18097-frito-lay-crunch-pop-mix-variety-pack-sack-recall-undeclared. Based on FDA recall #F-0690-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0690-2019%22&limit=1).

Why it’s dangerous

The popcorn bags may contain cheese-flavored chips that have undeclared milk. This can cause allergic reactions in individuals sensitive to dairy products who might not be aware of the milk content.

Who’s affected

People with dairy allergies who consume the recalled popcorn may be at risk due to undeclared milk. The recall affects consumers who bought the product between December 18, 2018, and January 1, 2019.

How to tell if you have this one

Check for 16-count Crunch & Pop Mix Variety Packs with use-by dates from December 18, 2018, to January 1, 2019. Look for a 11-digit manufacturing code starting with 'xAM' in the second and third positions.

  • Brand
    Frito-Lay
  • Category
    Food
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class I
  • Status
    Terminated
  • Distribution
    Alabama, Arkansas, Colorado, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Michigan, Minnesota, Missouri, Mississippi, North Carolina, North Dakota, Nebraska, New Mexico, Ohio, Oklahoma, South Carolina, South Dakota, Tennessee, Texas, Virginia, Wisconsin, West Virginia and Wyoming.
Recall numberProduct, codes & lots
F-0689-201916 count Smartfood Delight Variety Pack Sack; use by dates of 4 DEC 2018 OR 18 DEC 2018, and 11-digit manufacturing code that will include the letter combination AM in the second and third position (example: xAMxxxxxxxx)
F-0690-201916 count Crunch & Pop Mix Variety Pack Sack; use by dates of 18 DEC 2018 OR 1 JAN 2019, and 11-digit manufacturing code that will include the letter combination AM in the second and third position (example: xAMxxxxxxxx)
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for use-by dates from December 18, 2018, to January 1, 2019 and a 11-digit manufacturing code starting with 'xAM' in the second and third positions.

Where it went and when

Where it was distributed

Distributed in 29 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: not listedDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: not listedHITexas: yesTXFlorida: yesFL

FDA distribution: “Alabama, Arkansas, Colorado, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Michigan, Minnesota, Missouri, Mississippi, North Carolina, North Dakota, Nebraska, New Mexico, Ohio, Oklahoma, South Carolina, South…” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Alabama, Arkansas, Colorado, Florida, Georgia, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Michigan, Minnesota, Mississippi, Missouri, Nebraska, New Mexico, North Carolina, North Dakota, Ohio, Oklahoma, South Carolina, South Dakota, Tennessee, Texas, Virginia, West Virginia, Wisconsin, Wyoming.

Recall timeline

FDA terminated this recall 3 months after the firm started it.

1. Firm started the recall: Nov 2, 201812. FDA classified it Class I: Dec 4, 201823. Published in FDA’s Enforcement Report: Dec 12, 201834. FDA terminated the recall: Feb 5, 2019420182019
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Questions people ask

What should I do if I have this product?

Check the use-by date and manufacturing code. If it matches the recall criteria, contact Frito-Lay for a refund or replacement.

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Where this comes from

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.

  • Official source: FDA Recall #F-0690-2019 (November 2, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0690-2019 to see it in context.
  • Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA