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Lower risk Food recall · FDA · Published March 3, 2026

Frito-Lay Miss Vickies Spicy Dill Pickle Recall: Undeclared Milk Allergen

Frito-Lay recalls Miss Vickies Spicy Dill Pickle 8oz bags with undeclared milk allergen. Consumers should check for specific manufacturing codes and contact Frito-Lay for details.

🇺🇸 FDA recall #H-0571-2026FoodFrito-Lay ›
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Contact the company

Recalling firmFRITO-LAY NORTH AMERICA, INC.7701 Legacy Dr · Plano, TX 75024-4002
✎ GovInfoNow plain-language explainer

Frito-Lay is recalling Miss Vickies Spicy Dill Pickle 8-ounce bags due to an undeclared milk allergen. This poses a risk for people with milk allergies who may experience allergic reactions if they consume the product. Read more at govinfonow.com/recall/6682-frito-lay-miss-vickies-spicy-dill-pickle-recall-undeclared-milk.

Source Summary by GovInfoNow · govinfonow.com/recall/6682-frito-lay-miss-vickies-spicy-dill-pickle-recall-undeclared-milk · Updated August 18, 2026 · Official notice: FDA #H-0571-2026

Cite this page

“Frito-Lay Miss Vickies Spicy Dill Pickle Recall: Undeclared Milk Allergen.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/6682-frito-lay-miss-vickies-spicy-dill-pickle-recall-undeclared-milk. Based on FDA recall #H-0571-2026.

Frito-Lay North America, Inc. voluntarily recalled Miss Vickies Spicy Dill Pickle 8 oz bags due to undeclared milk allergens, according to the FDA on March 3, 2026.

How to tell if you have it

  • Brand: Miss Vickies
  • Product: Spicy Dill Pickle; 8 oz bag
  • "Guaranteed Fresh" date: 21 APR 2026
  • Manufacturing Codes: 38U301414, 48U101514

The hazard

The product contains undeclared milk, posing a risk to consumers with milk allergies. The FDA classified this as a Class I recall.

Context

GovInfoNow's records show the brand has been involved in other recent recalls of similar products including B.C. Williams Bakery Bread Mix Recall (2025-12-23) and Wawa Fruit Punch Pint Recall (2026-04-02). Other recent recalls of similar products include B.C. Williams Bakery Spice Cake Mix Recall (2025-12-23).

How to tell if you have this one

Check for the 8-ounce bag with a 'Guaranteed Fresh' date of April 21, 2026, and one of the manufacturing codes 38U301414 or 48U101514.

  • Brand
    Frito-Lay
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the 8-ounce bag with a 'Guaranteed Fresh' date of April 21, 2026, and one of the manufacturing codes 38U301414 or 48U101514.

Where it went and when

Where it was distributed

Distributed in 6 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: yesNMKansas: not listedKSArkansas: yesARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: yesTXFlorida: not listedFL

FDA distribution: “Arkansas, Louisiana, Mississippi, New Mexico, Oklahoma, and Texas.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arkansas, Louisiana, Mississippi, New Mexico, Oklahoma, Texas.

Recall timeline

FDA terminated this recall 2 months after the firm started it.

1. Firm started the recall: Mar 3, 202612. FDA classified it Class I: Mar 17, 202623. Published in FDA’s Enforcement Report: Mar 25, 202634. FDA terminated the recall: May 12, 202642026
  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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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 #H-0571-2026 (March 3, 2026)
  • Plain-language summary written by qwen3:4b on August 18, 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