The Ampt Life, LLC recalls NATURAL HERBAL COFFEE AMPT, sold in 25g packages (UPC 6942630905), 10-count packages per box (UPC 6942630912);
FDA recalls Ampt Natural Herbal Coffee due to undeclared sildenafil, tadalafil, and milk. This unapproved drug poses anaphylaxis risk for milk-allergic individuals. Stop using immediately.
Stop using this now
Marketed Without An Approved NDA/ANDA: FDA analysis found the product to contain undeclared sildenafil and tadalafil and undeclared milk. The presence of sildenafil and tadalafil makes AMPT Natural Herbal Coffee an unapproved drug for which safety and efficacy have not been established and, therefore, subject to recall. Additionally, this product has been found to contain undeclared milk, milk is recognized as one of the foods reported to have caused deaths due to anaphylactic shock in persons with underlying hypersensitivities.
Contact the company & request your remedy
What happened, in plain English
The FDA has recalled Ampt Natural Herbal Coffee products because they contain undeclared sildenafil and tadalafil, which are unapproved drugs. The product also contains undeclared milk, which can cause anaphylactic shock in people with milk allergies. Read more at govinfonow.com/recall/41422-ampt-natural-herbal-coffee-recall-unapproved-drugs-and-milk-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/41422-ampt-natural-herbal-coffee-recall-unapproved-drugs-and-milk-risk · Updated October 7, 2026 · FDA enforcement record: FDA #D-0126-2018
Cite this page
“Ampt Natural Herbal Coffee Recall: Unapproved Drugs and Milk Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/41422-ampt-natural-herbal-coffee-recall-unapproved-drugs-and-milk-risk. Based on FDA recall #D-0126-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0126-2018%22&limit=1).
Why it’s dangerous
The product contains undeclared sildenafil and tadalafil, which are prescription drugs not approved by the FDA. These substances can cause serious health risks. Additionally, the presence of undeclared milk poses a risk of anaphylactic shock for individuals with milk allergies.
Who’s affected
Anyone who owns or uses the recalled Ampt Natural Herbal Coffee products. People with milk allergies are at highest risk due to the undeclared milk.
How to tell if you have this one
Check for the product names 'NATURAL HERBAL COFFEE AMPT' sold in 25g packages (UPC 6942630905) or 10-count packages per box (UPC 6942630912). All lots of these products are affected.
- Brand
Ampt Life- Product
NATURAL HERBAL COFFEE AMPT, sold in 25g packages (UPC 6942630905), 10-count packages per box (UPC 6942630912)- Category
Drug
What to do — step by step
Stop Using Immediately
Discard all recalled Ampt Natural Herbal Coffee products to avoid exposure to undeclared sildenafil, tadalafil, and milk.
Questions people ask
Why was this product recalled?
The FDA found the product contains undeclared sildenafil and tadalafil, which are unapproved drugs, and undeclared milk that can cause anaphylactic shock in milk-allergic individuals.
What is the risk of using this product?
The product contains undeclared prescription drugs that have not been safety-tested, and milk that can cause life-threatening allergic reactions in people with milk allergies.
How can I tell if I have the recalled product?
Check for the product names 'NATURAL HERBAL COFFEE AMPT' sold in 25g packages (UPC 6942630905) or 10-count packages per box (UPC 6942630912).
Contact Ampt Life
We’ve drafted a message you can send Ampt Life to request your refund or repair — edit it as you like.
Subject: Recall D-0126-2018 — Ampt Life NATURAL HERBAL COFFEE AMPT, sold in 25g packages (UPC 6942630905), 10-count packages per Hello, I own a NATURAL HERBAL COFFEE AMPT, sold in 25g packages (UPC 6942630905), 10-count packages per box (UPC 6942630912) that is covered by recall D-0126-2018 from Ampt Life. 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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Where this comes from
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.
- Official source: FDA Recall #D-0126-2018 (August 1, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0126-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.