Food Recall Check
Class II · Moderate risk Terminated Initiated Apr 18, 2024 (2 years ago)

Longreen Corporation 4 in1 Reishi Coffee recall

Recalled by BF Suma Pharmaceuticals, Inc. · Rosemead, CA, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

Undeclared allergen: Soy

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

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

Quantity: 59,873 boxes

Food: Juice & beverages

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

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

California Texas

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

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to soy; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
BF Suma Pharmaceuticals, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Apr 18, 2024
In FDA report of
May 8, 2024
Terminated
Oct 9, 2024
FDA recall number
F-1206-2024 · event 94434
Official record
FDA enforcement report search

Also recalled with it (2 more products)

FDA files each product of one recall action separately; these share the same FDA event.

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