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Stop using now Food recall · FDA · Published October 10, 2018

Meiqili Durian Candy Recall: Undeclared Milk Allergy Risk

Fine Land Corp recalls Meiqili Durian Candy due to undeclared milk. Check your plastic bag with clear window for UPC 4-897055-795465-0.

🇺🇸 FDA recall #F-0794-2019FoodMeiqili ›
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Recalling firmFine Land Corp376 Vernon Ave · Brooklyn, NY 11206-6702
✎ GovInfoNow plain-language explainer

What happened, in plain English

Fine Land Corp is recalling Meiqili Durian Candy because it contains undeclared milk. This poses a risk to anyone with a milk allergy who might consume the product unknowingly. The candy comes in a plastic bag with a clear window and has a net weight of 12 ounces (340 g). Read more at govinfonow.com/recall/18413-meiqili-durian-candy-recall-undeclared-milk-allergy-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/18413-meiqili-durian-candy-recall-undeclared-milk-allergy-risk · Updated October 11, 2026 · FDA enforcement record: FDA #F-0794-2019

Cite this page

“Meiqili Durian Candy Recall: Undeclared Milk Allergy Risk.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/18413-meiqili-durian-candy-recall-undeclared-milk-allergy-risk. Based on FDA recall #F-0794-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0794-2019%22&limit=1).

Why it’s dangerous

The undeclared milk can cause serious allergic reactions in individuals sensitive to dairy products. Because the ingredient is not listed on the label, consumers cannot avoid it by reading the packaging.

Who’s affected

Consumers who purchased Meiqili Durian Candy, particularly those with milk allergies or sensitivities. The product was distributed in Connecticut, New York, Philadelphia, Virginia, Maryland, and Massachusetts.

How to tell if you have this one

Look for Meiqili Durian Candy in a plastic bag with a clear window. The package should be labeled as a product of P.R.C., have a net weight of 12 ounces (340 g), and display the UPC code 4-897055-795465-0.

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

What to do — step by step

  1. Stop consuming the candy

    Do not eat the Meiqili Durian Candy if you have a milk allergy or suspect it may contain undeclared milk.

  2. Check your product details

    Verify if your package matches the description: plastic bag with clear window, 12 oz weight, and UPC 4-897055-795465-0.

Where it went and when

Where it was distributed

Distributed in 5 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: not listedNJConnecticut: yesCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: yesVAMaryland: yesMDDelaware: 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: “Connecticut, New York, Philadelphia, Virginia, Maryland and Massachusetts” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Connecticut, Maryland, Massachusetts, New York, Virginia.

Recall timeline

FDA terminated this recall 4 months after the firm started it.

1. Firm started the recall: Oct 10, 201812. FDA classified it Class I: Feb 1, 201923. FDA terminated the recall: Feb 5, 201934. Published in FDA’s Enforcement Report: Feb 6, 2019420182019
  1. Firm started the recall
  2. FDA classified it Class I
  3. FDA terminated the recall
  4. Published in FDA’s Enforcement Report

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-0794-2019 (October 10, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0794-2019 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