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

Apollo Food Mini Roll Recall: Undeclared Eggs in Product

Apollo Food recalls Mini Roll snacks due to undeclared eggs. Products sold in pink 2.469 oz plastic packages with 2018.03.20 production date. Consumers should check for this specific packaging.

🇺🇸 FDA recall #F-0350-2019FoodApollo Food ›
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Recalling firmAPOLLO FOOD INTERNATIONAL INC.3710 Review Ave · Long Island City, NY 11101-2018
✎ GovInfoNow plain-language explainer

What happened, in plain English

Apollo Food is recalling Mini Roll snacks because they contain undeclared eggs. This means people with egg allergies could be at risk of an allergic reaction. The recall applies to specific packaging with a 2018.03.20 production date. Read more at govinfonow.com/recall/18445-apollo-food-mini-roll-recall-undeclared-eggs-in-product.

Source Summary by GovInfoNow · govinfonow.com/recall/18445-apollo-food-mini-roll-recall-undeclared-eggs-in-product · Updated October 6, 2026 · FDA enforcement record: FDA #F-0350-2019

Cite this page

“Apollo Food Mini Roll Recall: Undeclared Eggs in Product.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/18445-apollo-food-mini-roll-recall-undeclared-eggs-in-product. Based on FDA recall #F-0350-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0350-2019%22&limit=1).

Why it’s dangerous

The product contains undeclared eggs, meaning it may cause allergic reactions in people who are sensitive to eggs. This is a food safety issue that could lead to health problems for those with egg allergies.

Who’s affected

People who purchased the Mini Roll snacks with a 2018.03.20 production date in pink 2.469 ounce plastic packaging are affected. Those with egg allergies are most at risk of an allergic reaction.

How to tell if you have this one

Check for Mini Roll snacks in a 2.469 ounce pink plastic package with a production date of 2018.03.20 stamped on the back. The product UPC code is 6946050104746.

  • Brand
    Apollo Food
  • Product
    Mini Roll, The product comes in a 2.469 ounce pink plastic package marked with a production date of 2018.03.20 stamped
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Packaging

    Look for the 2.469 ounce pink plastic package with a production date of 2018.03.20 on the back.

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: not listedILWisconsin: not listedWIMichigan: not listedMINew York: yesNYRhode Island: not listedRIMassachusetts: yesMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: yesNJConnecticut: 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: 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: “MA, NY, NJ” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Massachusetts, New Jersey, New York.

Recall timeline

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

1. Firm started the recall: Oct 2, 201812. FDA classified it Class I: Nov 1, 201823. Published in FDA’s Enforcement Report: Nov 7, 201834. FDA terminated the recall: Feb 20, 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

Is there a risk of serious injury?

No, the recall is for people with egg allergies, not a physical hazard that causes injury.

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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-0350-2019 (October 2, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0350-2019 to see it in context.
  • Plain-language summary written by qwen3:4b on October 6, 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