Unrated Drug recall · FDA · Published May 6, 2019

Stiff Boy The Beast Recall: Undeclared Sildenafil Risk for Heart Disease

Stiff Boy LLC recalls The Beast pills due to undeclared sildenafil found in FDA analysis. Risk of heart issues from unapproved medication. No remedy stated in recall notice.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #D-1321-2019Drug Stiff Boy ›

Recall notice

Marketed without an Approved NDA/ANDA: The Beast contains undeclared sildenafil which was discovered through FDA analysis.

Take action

Contact the company

Recalling firmStiff Boy LLC90 Highwood Ave · Englewood, NJ 07631-1717

✎ GovInfoNow plain-language explainer

Stiff Boy LLC is recalling The Beast pills because they contain undeclared sildenafil, a drug not approved for heart disease treatment. This poses a risk of heart problems since the product was marketed without FDA approval. Read more at govinfonow.com/recall/38827-stiff-boy-the-beast-recall-undeclared-sildenafil-risk-for-heart.

Source Summary by GovInfoNow · govinfonow.com/recall/38827-stiff-boy-the-beast-recall-undeclared-sildenafil-risk-for-heart · Updated October 5, 2026 · FDA enforcement record: FDA #D-1321-2019

Cite this page

“Stiff Boy The Beast Recall: Undeclared Sildenafil Risk for Heart Disease.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/38827-stiff-boy-the-beast-recall-undeclared-sildenafil-risk-for-heart. Based on FDA recall #D-1321-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1321-2019%22&limit=1).

The FDA announced on May 6, 2019, that Stiff Boy LLC voluntarily recalled The Beast, a drug marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA). The product contains undeclared sildenafil. Owners should stop using the product immediately.

How to tell if you have it

Brand: Stiff Boy
Product name: The Beast
Description: The Beast can be taken under the situation of Heart disease and even after drinking, 4600 mg X 4 Capsules per packet
Quantity: 1000 boxes
Distribution: Nationwide

The hazard

The Beast contains undeclared sildenafil which was discovered through FDA analysis. The product is marketed without an Approved NDA/ANDA.

Context

Other recent recalls of similar products include StuffbyNainax MR 7 SUPER 700000 Capsules (2025-12-15) and Shoolin Pharma Chem Sildenafil Recall (2026-08-03). Buy-Herbal Kian Pee Wan Capsules Recall occurred on 2026-03-21.

How to tell if you have this one

The Beast pills are sold by Stiff Boy LLC. All lots are affected. The product is marketed for heart disease and can be taken after drinking, with 4600 mg per 4 capsules.

Brand
Stiff Boy
Category
Drug

Based on the official FDA remedy

What to do — step by step

Check Product Details
Look for The Beast pills with the description '4600 mg X 4 Capsules per packet' sold by Stiff Boy LLC.

Where it went and when

Where it was distributed

Distributed nationwide.

FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 6.4 years after the firm started it.

May 6, 2019Firm started the recall
Jun 5, 2019FDA classified it Class I
Jun 5, 2019Published in FDA’s Enforcement Report
Sep 16, 2025FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Link to this recall

<a href="https://govinfonow.com/recall/38827-stiff-boy-the-beast-recall-undeclared-sildenafil-risk-for-heart">Stiff Boy The Beast Recall: Undeclared Sildenafil Risk for Heart Disease (GovInfoNow)</a>

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-1321-2019 (May 6, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1321-2019 to see it in context.
Plain-language summary written by qwen3:4b on October 5, 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.