Skip to content
Lower risk Food recall · FDA · Published May 18, 2018

Hee Chang Green Tea Latte Recall: Allergen Not Declared

Hee: Hee Chang Dairy & Food Co., LTD recalls Green Tea Latte packets due to failure to declare allergens during FDA inspection. Products contain lactose and may cause allergic reactions.

🇺🇸 FDA recall #F-1618-2018FoodHee Chang ›
Take action

Contact the company

Recalling firmHee Chang Dairy & Food Co., LTD45 Yusangongdan7-Gil · Yangsan, Korea (the Republic of)
✎ GovInfoNow plain-language explainer

What happened, in plain English

Hee Chang Dairy & Food Co., LTD is recalling Green Tea Latte packets because they did not declare allergens during a FDA inspection. This could cause allergic reactions for people sensitive to lactose or other ingredients. Read more at govinfonow.com/recall/19113-hee-chang-green-tea-latte-recall-allergen-not-declared.

Source Summary by GovInfoNow · govinfonow.com/recall/19113-hee-chang-green-tea-latte-recall-allergen-not-declared · Updated October 7, 2026 · FDA enforcement record: FDA #F-1618-2018

Cite this page

“Hee Chang Green Tea Latte Recall: Allergen Not Declared.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19113-hee-chang-green-tea-latte-recall-allergen-not-declared. Based on FDA recall #F-1618-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1618-2018%22&limit=1).

Why it’s dangerous

The FDA found that four products did not declare allergens during a foreign inspection. This means the packets may contain lactose and other allergens without proper labeling, which could cause allergic reactions in sensitive individuals.

Who’s affected

People who own or use the recalled Green Tea Latte packets are at risk if they have allergies to lactose or other ingredients listed. Those with severe allergies may experience reactions.

How to tell if you have this one

Look for Green Tea Latte packets labeled '35.3 oz. (1 kg)' with lot number 20161125 and expiration date 2018.11.24. The product was imported and distributed by Coffee Tree USA in Los Angeles, CA.

  • Brand
    Hee Chang
  • Category
    Food
FDA recall event · 4 products

All 4 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Status
    Terminated
  • Distribution
    One US Customer in CA
Recall numberProduct, codes & lotsQuantityClass
F-1615-2018Black Bean Cereal Latte; 28.2 oz. package Ingredients: Non Dairy Creamer (corn syrup, vegetable oil, Sodium Caseinate, Silicon dioxide), Rice Powder, Bean Powder, Silicon dioxide, Refined Salt, Black Sesame. Corn syrup 57% Hydrogenated coconut oil 28% Sweet whey powder 10% (the firm said this is 100% pure whey/milk ingredient) Sodium caseinate 1.3%. Imported and Distributed by: Coffee Tree USA 2203W Venice Blvd, Unit 101A Los Angeles, CA 90006 USA; Lot 20170206; Exp date 2018.08.05468 boxes total - all productsClass I
F-1616-2018Black Bean Job's Tears Tea, 35.3 oz. (KG) package Ingredients: Non Dairy Creamer (corn syrup, Palm oil, Lactose, Whey Powder, Dipotassium Phosphate, Silicon dioxide, Refined Salt, Milk flavor), citron Syrup, Rice, Job's Tears Corn, Black Bean Powder, guar gum. The non-dairy creamer ingredient comprises 36% of the finished product; and contains the following sub ingredients: Corn syrup 72% Palm oil 20% Sweet whey powder 4% (the firm said this is 100% pure whey/milk ingredient) Lactose 2% Soy lecithin 0.3 % Imported and Distributed by: Coffee Tree USA 2203W Venice Blvd, Unit 101A Los Angeles, CA 90006 USA; Lot 20170121; Exp date 2018.07.20468 boxes total, all productsClass II
F-1617-2018Citron Tea; 35.3 oz. (1 kg) packet Ingredients: White Sugar, Dried Citron Powder, Citric Acid, carboxymethylcellulose, Sodium citrate; Silicon dioxide, Citron Flavor. Citron Powder contains corn syrup 58% and Lactose 20% Imported and Distributed by: Coffee Tree USA 2203W Venice Blvd, Unit 101A Los Angeles, CA 90006 USA; Lot 20170131; Exp date 2019.01.30468 boxes, all productsClass II
F-1618-2018Green Tea Latte; 35.3 oz. (1 kg) packet Ingredients: White sugar, Instant Whole Milk Powder (Corn Syrup, Milk cream, Lactose, Lecithin, Sodium Caseinate, Non Dairy Creamer (corn Syrup, vegetable oil, sodium caseinate, Silicon Dioxide, Skim Milk Powder, Whey Powder, Green Tea Powder, Whipped Cream Powder Citron Powder contains corn syrup 58% and Lactose 20% Imported and Distributed by: Coffee Tree USA 2203W Venice Blvd, Unit 101A Los Angeles, CA 90006 USA; Lot 20161125; Exp date 2018.11.24468 boxes, all productsClass II
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the lot number 20161125 and expiration date 2018.11.24 on the Green Tea Latte packet.

Where it went and when

Where it was distributed

Distributed in California.

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: yesCAUtah: 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: “One US Customer in CA” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California.

Recall timeline

FDA terminated this recall 11 months after the firm started it.

1. Firm started the recall: May 18, 201812. FDA classified it Class II: Jul 10, 201823. Published in FDA’s Enforcement Report: Jul 18, 201834. FDA terminated the recall: Apr 26, 2019420182019
  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.

✎ GovInfoNow

Questions people ask

Is there a risk of serious injury?

The recall is for allergen labeling issues, which could cause allergic reactions but not serious injury in normal use.

Similar recalls

Latest food recalls

Keep exploring

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-1618-2018 (May 18, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1618-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on October 7, 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