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Tonight We Ride, LLC announced a voluntary recall of all lots of Ultimate Forza Male Supplement capsules after third-party testing found undeclared sildenafil, tadalafil and dapoxetine. The products were sold at certain independently operated GNC franchise locations from 2017 through October 1, 2026; the company says no adverse events or complaints have been reported to date.
Tonight We Ride, LLC is recalling all lots of its Ultimate Forza Male Supplement capsules after third-party testing identified undeclared sildenafil, tadalafil and dapoxetine, according to the company announcement posted by the FDA on October 24, 2026. The company says the products were distributed through certain independently owned GNC franchise locations and advises consumers to stop using them.
The recall covers two configurations: Ultimate Forza Multi-Capsule/Box, item number 810208, UPC 868592000002, and Ultimate Forza Single Pack, item number 810222, UPC 868592000040. The box contains ten blue hard-shell capsules; the single pack contains one. The announcement says affected products were distributed through certain independent GNC franchise locations in the United States from 2017 to October 1, 2026. They were not sold through GNC corporate stores.
The company says the recall followed third-party product testing by GNC, which detected all three ingredients. According to the announcement, sales were stopped, affected stock was quarantined at franchise locations, and customers were notified to discontinue use and return remaining product. The company reports that no adverse events or complaints have been reported to date; that statement describes reports received by the company and does not establish that no consumer has experienced a problem.
Consumers are advised to stop using the supplement immediately. Unopened or partially used product may be returned to a GNC store for a full refund. The announcement says customers should provide a receipt or the phone number or email address connected to the loyalty account used for the purchase so it can be verified. Questions can be directed to GNC Customer Service at 1-877-462-4700 or GNCRecalls@gnc-hq.com.
Undeclared Ingredients Pose Drug Risks
The ingredients matter because sildenafil and tadalafil are active ingredients in FDA-approved prescription drugs used to treat erectile dysfunction, while the recalled supplement was marketed as a male performance dietary supplement. The FDA-posted announcement says the presence of these undeclared substances makes the product an unapproved drug whose safety and efficacy have not been established for this use.
The announcement warns that sildenafil and tadalafil may interact with nitrates in some prescription medicines, including nitroglycerin, and may lower blood pressure to dangerous levels. People with conditions such as diabetes, high blood pressure, high cholesterol or heart disease may take nitrate medicines, according to the notice. Consumers who used the product and have concerns or symptoms should contact a physician or other healthcare provider.
The notice also states that dapoxetine is not approved by the U.S. FDA and that its safety and efficacy have not been established by the agency. It says consumption has been shown to increase the risk of suicidal thinking and behavior in children, adolescents and young adults. The announcement does not provide a product-specific estimate of risk or report that such effects occurred among Ultimate Forza users.
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How Testing Prompted the Recall
The FDA page identifies this as a company announcement posted as a public service. It says the FDA does not endorse the product or the company. The recall was announced by Tonight We Ride, LLC, of Lakeville, Minnesota, and applies to all lots of the named capsules, rather than a single identified batch.
The products were sold through certain independently owned and operated GNC franchise locations—not GNC corporate stores—over a distribution period running from 2017 to October 1, 2026. The company’s notice says GNC’s third-party testing found the undeclared ingredients. It does not provide further details about the testing method, when the samples were collected, or how many units were distributed.
““The presence of Sildenafil, Tadalafil, and Dapoxetine in this product renders them unapproved drugs for which the safety and efficacy have not been established.””
— Tonight We Ride, LLC, in its recall announcement
Distribution Scope and Health Reports
The notice does not state how many packages were distributed or sold, identify the specific franchise locations, or say how many products have been returned. It also does not provide the testing results, the amount of each ingredient found, or the method used to test the capsules.
Although the company says no adverse events or complaints have been reported to date, the announcement does not specify how that information was gathered or whether any reports have since been received. Consumers’ individual exposure and health risks are not detailed in the notice. The company and FDA posting also do not describe any separate enforcement action or investigation beyond the announced recall.
Returns and Safety Reporting
Consumers who have either recalled configuration should stop taking it and return it to a GNC store for a full refund. A receipt or the phone number or email address linked to the purchase’s loyalty account can help verify the transaction. Customers with questions can contact GNC at 1-877-462-4700 or GNCRecalls@gnc-hq.com.
Anyone who believes they experienced a problem after using the product should contact a physician or healthcare provider, as the company advises. Consumers may also report adverse reactions or quality problems to the FDA’s MedWatch program online at www.fda.gov/medwatch/report.htm. The announcement does not give a deadline for returns or say when the recall process will be complete.
Key Questions
Which Ultimate Forza products are included in the recall?
The recall covers all lots of the Ultimate Forza Multi-Capsule/Box, item 810208, UPC 868592000002, and Ultimate Forza Single Pack, item 810222, UPC 868592000040.
Where were the recalled products sold?
The company says they were distributed through certain independently owned and operated GNC franchise locations in the United States from 2017 to October 1, 2026. They were not sold through GNC corporate stores.
What should consumers do with the product?
Stop using it immediately and return unopened or partially used product to a GNC store for a full refund. Bring a receipt or provide the phone number or email address associated with the purchase’s loyalty account to help verify it.
What ingredients were found, and what risks does the notice describe?
Testing identified undeclared sildenafil, tadalafil and dapoxetine. The company notice warns that sildenafil and tadalafil may interact with nitrates and lower blood pressure to dangerous levels. It says dapoxetine is not FDA-approved and its safety and efficacy have not been established.
Have consumers reported adverse events?
The company says no adverse events or complaints have been reported to date. Consumers who experienced a problem should contact a healthcare provider and may report it to the FDA’s MedWatch program.
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