FDA recall record
Longreen Corporation 4 in1 Reishi Coffee, 18.2 grams/sachet, 10 sachets/box
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of October 9, 2024. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Longreen Corporation 4 in1 Reishi Coffee, 18.2 grams/sachet, 10 sachets/box
Reason
Undeclared allergens due to sub-ingredients, soy lecithin and coconut oil
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
Longreen Corporation 4 in1 Reishi Coffee, 18.2 grams/sachet, 10 sachets/box
Code information listed by FDA
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
Distribution and firm information
Recalling firm listed by FDA: BF Suma Pharmaceuticals, Inc.
Firm location listed by FDA: Rosemead, CA, United States
Distribution reported by FDA: U.S. distribution to the following states: CA, TX. Foreign distribution to Canada and Guatemala.
Product quantity listed by FDA: 59,873 boxes
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.