Class IIFood recall: undeclared soy
Longreen Corporation 4 in1 Reishi Coffee and 2 more products
BF Suma Pharmaceuticals, Inc., of Rosemead, CA, began recalling these 3 products on . FDA classified the recall as Class II on .
Why it was recalled
In FDA’s words:
Undeclared allergens due to sub-ingredients, soy lecithin and coconut oil
The allergen tags on this page are ours, matched from FDA’s words above.
The 3 products
Longreen Corporation 4 in1 Reishi Coffee
Longreen Corporation 4 in1 Reishi Coffee, 18.2 grams/sachet, 10 sachets/box
- Codes and dates
- 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
- Quantity
- 59,873 boxes
- Class
- Class II
- Recall number
- F-1206-2024
Longreen Corporation 4 in1 Cordyceps Coffee
Longreen Corporation 4 in1 Cordyceps Coffee, 18.2 grams/sachet, 10 sachets/box
- Codes and dates
- Batch No. C30919, Best By Date: 02 2026; Batch No. F34619, Best By Date: 05 2026; Batch No. F34719; Best By Date: 05 2026
- Quantity
- 15,528 boxes
- Class
- Class II
- Recall number
- F-1207-2024
Longreen Corporation Xlim Express Coffee
Longreen Corporation Xlim Express Coffee, 15 grams/sachet, 10 sachets/box
- Codes and dates
- Batch No. C33619, Best By Date: 02 2026; Batch No. H33119, Best By Date: 07 2026; Batch No. H33219, Best By Date: 07 2026; Batch No. C40719, Best By Date: 02 2027; Batch No. C40819, Best By Date: 02 2027
- Quantity
- 23,701 boxes
- Class
- Class II
- Recall number
- F-1208-2024
Where it was distributed
In FDA’s words:
U.S. distribution to the following states: CA, TX. Foreign distribution to Canada and Guatemala.
What Class II means
In FDA’s definitions, a Class II recall is one where: use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse health consequences is remote. FDA’s recall definitions
If you have this product
- FDA’s enforcement report doesn’t say what to do with a recalled product. FDA posts some companies’ recall announcements on its Recalls, Market Withdrawals and Safety Alerts page; not every recall has one.
- FDA doesn’t update a recall’s status after classifying it, so this page can’t tell you whether the recall is still open.
- If someone has a serious allergic reaction, call 911. Signs of a serious reaction
Source
FDA’s Enforcement Report, read through openFDA. This recall first appeared in the report of . openFDA asks that its data not be relied on for decisions about medical care. AllergyNest isn’t affiliated with or endorsed by FDA.