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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Food
Food & Beverages/Dietary Supplements

Longreen Corporation Coffee Products Recalled for Undeclared Soy and Coconut

Agency Publication Date: April 26, 2024
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Summary

BF Suma Pharmaceuticals, Inc. is recalling 99,102 boxes of various Longreen Corporation coffee products, including 4 in 1 Reishi Coffee, 4 in 1 Cordyceps Coffee, and Xlim Express Coffee. These products were distributed in California and Texas, as well as internationally in Canada and Guatemala. The recall was initiated because the products contain soy lecithin and coconut oil, which were not declared on the ingredient labels. No incidents or injuries have been reported to date regarding this issue.

Risk

People who have an allergy or severe sensitivity to soy or coconut run the risk of a serious or life-threatening allergic reaction if they consume these products. The sub-ingredients soy lecithin and coconut oil were missing from the product labels.

What You Should Do

  1. This recall affects Longreen Corporation coffee products sold in 10-sachet boxes, including the 4 in 1 Reishi, 4 in 1 Cordyceps, and Xlim Express varieties.
  2. Identify your product by checking the batch number and 'Best By' date printed on the packaging. See the Affected Products section below for the full list of affected codes.
  3. Return the product to the place of purchase for a refund, throw it away, or contact the manufacturer for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: Longreen Corporation 4 in 1 Reishi Coffee (18.2 grams/sachet, 10 sachets/box)by Longreen Corporation
Item Code:
F-1206-2024
Lot Numbers:
Batch No. A34319 (Exp 12/2025)
Batch No. A34419 (Exp 12/2025)
Batch No. E34519 (Exp 04/2026)
Batch No. E34619 (Exp 04/2026)
Batch No. F34119 (Exp 05/2026)
Batch No. F34219 (Exp 05/2026)
Batch No. H34519 (Exp 07/2026)
Batch No. H34619 (Exp 07/2026)
Batch No. A43119 (Exp 12/2026)
Batch No. A43219 (Exp 12/2026)
Batch No. B41119 (Exp 01/2027)
Batch No. B41219 (Exp 01/2027)

Quantity: 59,873 boxes

Product: Longreen Corporation 4 in 1 Cordyceps Coffee (18.2 grams/sachet, 10 sachets/box)by Longreen Corporation
Item Code:
F-1207-2024
Lot Numbers:
Batch No. C30919 (Exp 02/2026)
Batch No. F34619 (Exp 05/2026)
Batch No. F34719 (Exp 05/2026)

Quantity: 15,528 boxes

Product: Longreen Corporation Xlim Express Coffee (15 grams/sachet, 10 sachets/box)by Longreen Corporation
Item Code:
F-1208-2024
Lot Numbers:
Batch No. C33619 (Exp 02/2026)
Batch No. H33119 (Exp 07/2026)
Batch No. H33219 (Exp 07/2026)
Batch No. C40719 (Exp 02/2027)
Batch No. C40819 (Exp 02/2027)

Quantity: 23,701 boxes

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 94434
Status: Resolved
Manufacturer: BF Suma Pharmaceuticals, Inc.
Sold By: Longreen Corporation distributors
Manufactured In: United States
Units Affected: 3 products (59,873 boxes; 15,528 boxes; 23,701 boxes)
Distributed To: California, Texas

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.