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Use caution Food recall · FDA · Published November 8, 2017

Nestle Recalls Hot Pockets Due to Missing Allergen Labeling

Nestle USA is recalling Hot Pockets Four Cheese Pizza Snack Bites because they lack ingredient statements, posing an allergen risk.

🇺🇸 FDA recall #F-0606-2018FoodNestle ›
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Recalling firmNestle USA5750 Harper Rd · Solon, OH 44139-1831
✎ GovInfoNow plain-language explainer

What happened, in plain English

Nestle USA has recalled Hot Pockets Four Cheese Pizza Snack Bites sold in clear plastic bags. The product was distributed without the required ingredient statement or labeling. This omission means consumers cannot identify potential allergens contained within the food. Read more at govinfonow.com/recall/20059-nestle-recalls-hot-pockets-due-to-missing-allergen-labeling.

Source Summary by GovInfoNow · govinfonow.com/recall/20059-nestle-recalls-hot-pockets-due-to-missing-allergen-labeling · Updated October 11, 2026 · FDA enforcement record: FDA #F-0606-2018

Cite this page

“Nestle Recalls Hot Pockets Due to Missing Allergen Labeling.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/20059-nestle-recalls-hot-pockets-due-to-missing-allergen-labeling. Based on FDA recall #F-0606-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0606-2018%22&limit=1).

Why it’s dangerous

The product contains various allergens but lacks an ingredient statement on the packaging. Without this labeling, consumers with allergies may unknowingly consume ingredients that could cause a serious allergic reaction.

Who’s affected

Consumers who purchased Hot Pockets Four Cheese Pizza Snack Bites in clear plastic bags, specifically those in Missouri and Oklahoma. Individuals with food allergies are at risk because they cannot verify the ingredients.

How to tell if you have this one

Look for Hot Pockets Four Cheese Pizza Snack Bites in clear plastic bags. Check the batch code, which is 6327544616. The product was distributed to stores in Missouri and Oklahoma.

  • Brand
    Nestle
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check your product

    Verify if you have Hot Pockets Four Cheese Pizza Snack Bites in clear plastic bags with batch code 6327544616.

  2. Do not consume

    Because the product lacks ingredient labeling, do not eat it if you have allergies or cannot identify the contents.

Where it went and when

Where it was distributed

Distributed in Missouri and Oklahoma.

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: yesMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: yesOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “Product was sent to the following states: MO & OK” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Missouri, Oklahoma.

Recall timeline

FDA terminated this recall 7 months after the firm started it.

1. Firm started the recall: Nov 8, 201712. FDA classified it Class II: Jan 23, 201823. Published in FDA’s Enforcement Report: Jan 31, 201834. FDA terminated the recall: Jun 14, 2018420172018
  1. Firm started the recall
  2. FDA classified it Class II
  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 #F-0606-2018 (November 8, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0606-2018 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 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