Longreen Corporation 4 in1 Cordyceps Coffee, 18.2 grams/sachet, 10 sachets/box
Summary
The FDA issued a Class II for Longreen Corporation 4 in1 Cordyceps Coffee, 18.2 grams/sachet, 10 sachets/box by BF Suma Pharmaceuticals, Inc.. Reason: Undeclared allergens due to sub-ingredients, soy lecithin and coconut oil.
Details
Source
Food Recall
External ID
F-1207-2024
Action Date
2024-05-08
Status
Terminated
Category
food
Product Description
Longreen Corporation 4 in1 Cordyceps Coffee, 18.2 grams/sachet, 10 sachets/box
Lot/Code Info: 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 Affected: 15,528 boxes
Reason for Recall
Undeclared allergens due to sub-ingredients, soy lecithin and coconut oil
Distribution
U.S. distribution to the following states: CA, TX. Foreign distribution to Canada and Guatemala.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-04-18
Company
Rosemead, CA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 17 food recalls issued in the same week, part of 204 food-related FDA actions this month.
BF Suma Pharmaceuticals, Inc. has 3 FDA actions in our database, including 3 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (BF Suma Pharmaceuticals, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does BF Suma Pharmaceuticals, Inc. have FDA actions?
BF Suma Pharmaceuticals, Inc. has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1207-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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