Recall notice · FDA Recall Press Releases

STIFF BOY, LLC: FDA Recall Notice (May 7, 2019)

Agency action: May 7, 2019Record ID: fda_recall_p-b1f2802242339d1e
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What happened

Original notice title

STIFF BOY LLC. Issues Voluntary Nationwide Recall of THE BEAST Capsules Due to Presence of Undeclared Sildenafil

From the archived source record

This recall has been completed and FDA has terminated this recall. When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. More Recalls, Market Withdrawals, & Safety Alerts Recalls, Market Withdrawals, & Safety Alerts Recall Resources Enforcement Reports Industry Guidance For Recalls Major Product Recalls STIFF BOY LLC. is voluntarily recalling all lots within expiry of The Beast capsules to the consumer level. FDA analysis has found the product to be tainted with sildenafil. Sildenafil is an FDA approved drug for the treatment of male erectile dysfunction and is in a class of drugs called phosphodiesterase (PDE-5) inhibitors. The presence of sildenafil in THE BEAST Capsules renders it an unapproved drug for which safety and efficacy have not been established and, therefore, subject to recall. Consumption of a product with undeclared PDE-5 inhibitors may pose a threat to consumers because the active ingredients may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may lower blood pressure to dangerous levels which can be life threatening. Consumers with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates and may be the population most likely to be affected. To date, STIFF BOY LLC. has not received any reports of adverse events related to this recall. The product is marketed as a dietary supplement for male enhancement and is packaged in blue wrapping and blue box with an image of a beast, 4 capsules per package with no UPC barcode. All lots within expiry are being recalled. Product was distributed nationwide in the USA to online customers. STIFF BOY LLC is notifying its customers by email and is arranging for return of all recalled products.

What the official notice says to do

Check the original notice for the instructions that apply to the named product, company, and affected lots.

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Status and source details

Status recorded in the archive
Published recall notice
Source checked
Jul 16, 2026
Record revision
83b24d3c6c8f

This is a dated record. Its current status may have changed since the source was captured. A record applies to its stated scope; it is not a safety rating for every product from a company.

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What is affected

Product
THE BEAST capsules; STIFF BOY LLC. Issues Voluntary Nationwide Recall of THE BEAST Capsules Due to Presence of Undeclared Sildenafil
Company
STIFF BOY, LLC
Lot / identifier
The source does not specify this field.
Market / distribution
The source does not specify this field.