Longreen Corporation's 4-in-1 Cordyceps Coffee with undeclared soy lecithin and coconut oil poses allergy risks. Affected batches from 2025-2026 may cause allergic reactions. Consumers should check batch numbers and contact the company.
Undeclared allergens due to sub-ingredients, soy lecithin and coconut oil
Longreen Corporation's 4-in-1 Cordyceps Coffee, sold in 10-sachet boxes, contains undeclared allergens like soy lecithin and coconut oil. This could cause allergic reactions in sensitive individuals, so affected consumers should stop using the product.
The coffee contains soy lecithin and coconut oil without clear labeling, which can trigger allergic reactions in sensitive individuals. This is a food safety issue related to undeclared allergens.
Anyone who purchased Longreen 4-in-1 Cordyceps Coffee between 2025 and 2026, especially those with soy or coconut allergies. People with known allergies to these ingredients are most at risk.
Check the box for batch numbers: C30919 (best by 02/2026), F34619 (best by 05/2026), or F34719 (best by 05/2026). The product is sold in 10-sachet boxes labeled as 4-in-1 Cordyceps Coffee.
Look for batch numbers on the box: C30919, F34619, or F34719.
If you have the recalled batch, stop using the coffee immediately to avoid potential allergic reactions.
The coffee contains undeclared soy lecithin and coconut oil, which can trigger allergic reactions in sensitive individuals.
Check the box for batch numbers: C30919 (best by 02/2026), F34619 (best by 05/2026), or F34719 (best by 05/2026).
The recall record does not specify a return process, so contact Longreen Corporation directly for instructions.
We’ve drafted a message you can send Longreen Corporation to request your refund or repair — edit it as you like.
Subject: Recall F-1207-2024 — Longreen Corporation Longreen Corporation Hello, I own a Longreen Corporation that is covered by recall F-1207-2024 from Longreen Corporation. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
