TL;DR
Tonight We Ride, LLC announced a voluntary recall of all lots of Ultimate Forza Male Supplement capsules after testing found undeclared sildenafil, tadalafil and dapoxetine. The products were sold through certain independently owned GNC franchise locations in the United States from 2017 through October 1, 2026; consumers are advised to stop using them and can return them to a GNC store for a full refund.
Tonight We Ride, LLC is recalling all lots of its Ultimate Forza Male Supplement capsules after testing found undeclared sildenafil, tadalafil and dapoxetine, according to a company announcement posted by the FDA on October 24, 2026. The FDA says the ingredients can pose health risks, including potentially dangerous drops in blood pressure when sildenafil or tadalafil is taken with nitrate medicines.
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The recall covers two products: the Ultimate Forza Multi-Capsule/Box (item No. 810208, UPC 868592000002), containing 10 blue hard-shell capsules, and the Ultimate Forza Single Pack (item No. 810222, UPC 868592000040), containing one capsule. The supplements were marketed for male performance.
According to the company notice, the products were distributed from 2017 through October 1, 2026 through certain independently owned and operated GNC franchise locations in the United States. The notice says they were not sold through GNC corporate stores. GNC’s third-party product testing identified the undeclared ingredients, after which sales were stopped and affected stock was quarantined at franchise locations.
Customers who have the product should stop using it immediately. The company says unopened or partially used products may be returned to a GNC store for a full refund. To verify a purchase, customers should provide a receipt or the phone number or email address linked to the loyalty account used. The company announcement reports that no adverse events or complaints had been reported at the time of the notice.
Undeclared Drugs Carry Health Risks
The recall matters because the capsules contain prescription drug ingredients that were not declared on the product, so consumers may not know they are taking them or be able to check for medication interactions. The FDA announcement says sildenafil and tadalafil are active ingredients in FDA-approved prescription medicines for erectile dysfunction, whose use is restricted to supervision by a licensed health care professional.
The FDA 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 diabetes, high blood pressure, high cholesterol or heart disease may take nitrate medicines, according to the notice. Anyone who has used the supplement and is concerned about a possible reaction should contact a physician or other health care provider.
The third ingredient raises separate concerns. Dapoxetine is not approved by the U.S. FDA, and the agency says its safety and efficacy have not been established. The company notice also cites increased risk of suicidal thinking and behavior in children, adolescents and young adults associated with consumption. The notice does not establish that any particular consumer was harmed, and it reports no adverse events or complaints to date.
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How the Recall Was Triggered
The FDA page identifies this as a company announcement posted as a public service; it says the agency does not endorse the product or the company. The recall was initiated after GNC third-party testing found sildenafil, tadalafil and dapoxetine in Ultimate Forza, according to the company’s notice.
Tonight We Ride, based in Lakeville, Minnesota, said sales were stopped and products at affected franchise locations were quarantined. The notice says customers were notified to discontinue use and return remaining product. The distribution period listed in the announcement spans several years, from 2017 until October 1, 2026; the recall announcement itself was dated October 24, 2026.
““No adverse events or complaints have been reported to date.””
— Tonight We Ride, LLC, in the company announcement posted by the FDA
Scope and Health Effects Still Unknown
The announcement identifies the affected product configurations and distribution channel but does not provide lot numbers, quantities sold or the number of consumers reached. It also does not specify how many franchise locations carried the supplements. The listed distribution period ends October 1, 2026, while the recall was announced October 24.
The notice reports no adverse events or complaints at the time it was issued, but that statement does not rule out unreported effects. It does not say how much of each undeclared ingredient was present in the capsules or detail the testing results. The FDA page posts the company’s announcement and states that it does not endorse the product or company.
Returns and Health Reports
Consumers should stop taking the capsules and may return unopened or partially used product to a GNC store for a full refund. A receipt or the phone number or email address tied to the loyalty account used for purchase can help verify it. Questions can be directed to GNC Customer Service at 1-877-462-4700 or GNCRecalls@gnc-hq.com.
People who believe they have experienced a problem after using the supplement should contact a physician or health care provider. The FDA says adverse reactions or product-quality problems may also be reported through its MedWatch program online, by mail or by fax. The company notice does not give a deadline for returns or say whether additional testing or recall updates are planned.
Key Questions
Which Ultimate Forza products are included in the recall?
The recall covers all lots of the Multi-Capsule/Box (item No. 810208, UPC 868592000002) and Single Pack (item No. 810222, UPC 868592000040).
Where were the recalled supplements sold?
The company says they were distributed from 2017 through October 1, 2026 through certain independently owned and operated GNC franchise locations in the United States. The notice says they were not sold through GNC corporate stores.
What should consumers do with the product?
Stop using it immediately. Unopened or partially used product can be returned to a GNC store for a full refund. Bring a receipt or the phone number or email address associated with the purchase’s loyalty account for verification.
Why was Ultimate Forza recalled?
Third-party testing identified undeclared sildenafil, tadalafil and dapoxetine. The FDA notice warns that sildenafil and tadalafil may interact with nitrates and lower blood pressure to dangerous levels; it says dapoxetine is not approved by the U.S. FDA.
Who can consumers contact with questions or health concerns?
For recall questions, contact GNC Customer Service at 1-877-462-4700 or GNCRecalls@gnc-hq.com. For possible health effects, contact a physician or health care provider; adverse reactions can also be reported to the FDA’s MedWatch program.
Source: primary
