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Stop using now Food recall · FDA · Published September 21, 2018

Recall: Lic's Reese's Oreo Ice Cream Missing Peanut Warning

Lloyd's Ice Cream recalls Lic's Reese's Oreo Ice Cream because the label fails to declare peanuts, posing a risk to those with allergies.

🇺🇸 FDA recall #F-0027-2019FoodLic's ›
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Recalling firmLloyd'S Ice Cream Inc900 Vine St · Evansville, IN 47708-1944
✎ GovInfoNow plain-language explainer

What happened, in plain English

Lloyd's Ice Cream Inc is voluntarily recalling pre-packed quarts of Lic's Reese's Oreo Ice Cream. The product was recalled because the label does not declare peanuts as an ingredient. This omission poses a serious health risk to consumers with peanut allergies who may unknowingly consume the product. Read more at govinfonow.com/recall/18645-recall-lic-s-reese-s-oreo-ice-cream-missing-peanut.

Source Summary by GovInfoNow · govinfonow.com/recall/18645-recall-lic-s-reese-s-oreo-ice-cream-missing-peanut · Updated October 11, 2026 · FDA enforcement record: FDA #F-0027-2019

Cite this page

“Recall: Lic's Reese's Oreo Ice Cream Missing Peanut Warning.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/18645-recall-lic-s-reese-s-oreo-ice-cream-missing-peanut. Based on FDA recall #F-0027-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0027-2019%22&limit=1).

Why it’s dangerous

The product contains peanuts, but the label fails to list them as an ingredient. Consumers relying on the label for allergen information may ingest the product unknowingly, leading to potentially life-threatening allergic reactions.

Who’s affected

Consumers in Indiana and Kentucky who purchased Lic's Reese's Oreo Ice Cream between April 12, 2016, and September 17, 2018. Individuals with peanut allergies are at the highest risk of severe allergic reaction.

How to tell if you have this one

Check for Lic's brand Reese's Oreo Ice Cream in a plastic quart container (946 mL). Verify if the manufacturing date falls between April 11, 2016, and June 25, 2018. Look for one of the following codes on the packaging: 102, 123, 193, 235, 277, 37, 100, 191, 212, 310, 352, or 176.

  • Brand
    Lic's
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not eat the recalled ice cream if you have a peanut allergy or are unsure about ingredients.

  2. Check your packaging

    Verify the brand, container type, manufacturing dates, and codes against the recall details to confirm if your item is affected.

  3. Return or discard the product

    The record does not specify a return process or remedy for consumers; please contact Lloyd's Ice Cream Inc for further instructions.

Where it went and when

Where it was distributed

Distributed in Indiana and Kentucky.

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: yesINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: yesKYWest 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: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “Domestic Only: IN and KY” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Indiana, Kentucky.

Recall timeline

FDA terminated this recall 5 months after the firm started it.

1. Firm started the recall: Sep 21, 201812. FDA classified it Class I: Oct 11, 201823. Published in FDA’s Enforcement Report: Oct 17, 201834. FDA terminated the recall: Feb 8, 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.

✎ GovInfoNow

Questions people ask

Where was this product sold?

The product was distributed domestically only in Indiana and Kentucky.

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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-0027-2019 (September 21, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0027-2019 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