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Stop using now Food recall · FDA · Published June 30, 2016

Sundae Shoppe Ice Cream Cone Recall: Undeclared Peanuts

Aldi distributes Sundae Shoppe ice cream cones that may contain undeclared peanuts. Check your UPC for recall details.

🇺🇸 FDA recall #F-1915-2016FoodSundae Shoppe ›
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Contact the company

Recalling firmMister Cookie Face Corporation1989 Rutgers University Blvd · Lakewood, NJ 08701-4538
✎ GovInfoNow plain-language explainer

What happened, in plain English

Mister Cookie Face Corporation is recalling Sundae Shoppe Novelty Ice Cream Dipped "Variety" cones because they may contain peanuts that are not listed on the allergen statement. This poses a risk to individuals with peanut allergies who might consume the product unknowingly. The affected items were distributed in Illinois, North Carolina, and Ohio. Read more at govinfonow.com/recall/23907-sundae-shoppe-ice-cream-cone-recall-undeclared-peanuts.

Source Summary by GovInfoNow · govinfonow.com/recall/23907-sundae-shoppe-ice-cream-cone-recall-undeclared-peanuts · Updated October 9, 2026 · FDA enforcement record: FDA #F-1915-2016

Cite this page

“Sundae Shoppe Ice Cream Cone Recall: Undeclared Peanuts.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23907-sundae-shoppe-ice-cream-cone-recall-undeclared-peanuts. Based on FDA recall #F-1915-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1915-2016%22&limit=1).

Why it’s dangerous

The product is labeled as "Variety" but may contain peanuts that are not declared on the packaging. For people with severe peanut allergies, accidental ingestion can lead to serious allergic reactions or anaphylaxis.

Who’s affected

Consumers who purchased Sundae Shoppe ice cream cones from Aldi stores in Illinois, North Carolina, or Ohio are likely affected. Individuals with peanut allergies are at the highest risk of an allergic reaction.

How to tell if you have this one

Look for Sundae Shoppe Novelty Ice Cream Dipped "Variety" cones in a 32 oz. box. The UPC code is 041498191962. These products were manufactured by Mister Cookie Face LLC in Lakeland, NJ, and distributed by Aldi.

  • Brand
    Sundae Shoppe
  • Product
    Sundae Shoppe Novelty Ice Cream Dipped "Variety"cones, 32 oz. box, Manufactured by Mister Cookie Face LLC, Lakeland, NJ
  • Category
    Food

Where it went and when

Where it was distributed

Distributed in 3 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: 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: yesOHPennsylvania: 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: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: yesNCSouth 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: “IL, NC and OH” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Illinois, North Carolina, Ohio.

Recall timeline

FDA terminated this recall 9 months after the firm started it.

1. Firm started the recall: Jun 30, 201612. FDA classified it Class II: Aug 6, 201623. Published in FDA’s Enforcement Report: Aug 17, 201634. FDA terminated the recall: Apr 7, 2017420162017
  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-1915-2016 (June 30, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1915-2016 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 9, 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