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Class II: temporary or reversible health riskTerminated

BF Suma Pharmaceuticals Longreen Corporation 4 in1 Reishi Coffee Recall

Longreen Corporation 4 in1 Reishi Coffee, 18

BF Suma Pharmaceuticals, Inc. · Rosemead, CA

Risk level
Class II
Reported by FDA
May 8, 2024
Recall ID
F-1206-2024
Check your lot numberHow we source this data

Summary

BF Suma Pharmaceuticals recalled Longreen Corporation 4 in1 Reishi Coffee starting Apr 18, 2024. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-1206-2024 on May 8, 2024. Reason: Undeclared allergens due to sub-ingredients, soy lecithin and coconut oil. Status: Terminated.

Why it was recalled

Undeclared allergens due to sub-ingredients, soy lecithin and coconut oil

Product description

Longreen Corporation 4 in1 Reishi Coffee, 18.2 grams/sachet, 10 sachets/box

Lot numbers, UPCs & expiration codes

Batch No. A34319, Best By Date: 12 2025; Batch No. A34419, Best By Date: 12 2025; Batch No. E34519, Best By Date: 04 2026; Batch No. E34619, Best By Date: 04 2026; Batch No. F34119, Best By Date: 05 2026; Batch No. F34219, Best By Date: 05 2026; Batch No. H34519, Best By Date: 07 2026; Batch No. H34619, Best By Date: 07 2026; Batch No. A43119, Best By Date: 12 2026; Batch No. A43219, Best By Date: 12 2026; Batch No. B41119, Best By Date: 01 2027; Batch No. B41219, Best By Date: 01 2027

Where it was sold

U.S. distribution to the following states: CA, TX. Foreign distribution to Canada and Guatemala.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-1206-2024
Classification
Class II
Status
Terminated
Recall initiated
Apr 18, 2024
FDA report date
May 8, 2024
Quantity
59,873 boxes
Recall type
Voluntary: Firm initiated
Recalling firm
BF Suma Pharmaceuticals, Inc.

Original FDA data

Every field from FDA enforcement report F-1206-2024, exactly as published.

Show all FDA fields
City
Rosemead
State
CA
Status
Terminated
Country
United States
Event ID
94434
Address
5001 Earle Ave
Code information
Batch No. A34319, Best By Date: 12 2025; Batch No. A34419, Best By Date: 12 2025; Batch No. E34519, Best By Date: 04 2026; Batch No. E34619, Best By Date: 04 2026; Batch No. F34119, Best By Date: 05 2026; Batch No. F34219, Best By Date: 05 2026; Batch No. H34519, Best By Date: 07 2026; Batch No. H34619, Best By Date: 07 2026; Batch No. A43119, Best By Date: 12 2026; Batch No. A43219, Best By Date: 12 2026; Batch No. B41119, Best By Date: 01 2027; Batch No. B41219, Best By Date: 01 2027
Postal code
91770-1169
Report date
May 8, 2024
Product type
Food
Recall number
F-1206-2024
Classification
Class II
Recalling firm
BF Suma Pharmaceuticals, Inc.
Product quantity
59,873 boxes
Termination date
Oct 9, 2024
Reason for recall
Undeclared allergens due to sub-ingredients, soy lecithin and coconut oil
Voluntary / mandated
Voluntary: Firm initiated
Product description
Longreen Corporation 4 in1 Reishi Coffee, 18.2 grams/sachet, 10 sachets/box
Distribution pattern
U.S. distribution to the following states: CA, TX. Foreign distribution to Canada and Guatemala.
Recall initiation date
Apr 18, 2024
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Apr 26, 2024

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1206-2024, published May 8, 2024. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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