TL;DR
Get workout gear delivered free with Prime
- Fast, free delivery on millions of items
- Prime Video, Amazon Music and more included
- Member-only deals all year
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 distributed through some independently operated GNC franchise locations; consumers are advised to stop using them and may return them for a full refund.
Tonight We Ride, LLC is voluntarily recalling all lots of Ultimate Forza Male Supplement capsules after testing found undeclared sildenafil, tadalafil and dapoxetine, according to a company announcement posted by the U.S. Food and Drug Administration on October 24, 2026. The products were sold through certain independently owned GNC franchise locations, and consumers are advised to stop using them because the unlisted ingredients can pose health risks.
The recall covers two configurations: the Ultimate Forza Multi-Capsule/Box (item No. 810208, UPC 868592000002), containing ten blue hard-shell capsules, and the Ultimate Forza Single Pack (item No. 810222, UPC 868592000040), containing one capsule. The company said the products were distributed through certain independently operated GNC franchise locations in the United States from 2017 to October 1, 2026. They were not sold through GNC corporate stores.
According to the announcement, GNC third-party product testing identified the three undeclared ingredients, prompting the recall. Sales were stopped, affected products were quarantined at franchise locations, and customers were notified to discontinue use and return remaining product. The company said no adverse events or complaints had been reported as of the October 24 announcement.
Consumers should stop using the supplement immediately. The company says unopened or partially used products can be returned to a GNC store for a full refund. A receipt or the phone number or email address connected to the loyalty account used for the purchase should be provided to verify it. The FDA’s recall page republishes company announcements as a public service and says that posting does not mean the agency endorses a product or company.
The undeclared substances matter because consumers may take the capsules believing they are using a dietary supplement, without knowing they are also ingesting active drug ingredients. The company announcement says sildenafil and tadalafil are active ingredients in FDA-approved prescription drugs used to treat erectile dysfunction, and that those prescription medicines are intended for use under a licensed health care professional’s supervision.
The FDA-posted notice warns that sildenafil and tadalafil may interact with nitrates in some prescription medicines, including nitroglycerin, and may lower blood pressure to dangerous levels. It notes that people with diabetes, high blood pressure, high cholesterol or heart disease often take nitrates. People who have used the product and have concerns should speak with a physician or other health care provider rather than assume the supplement’s ingredients were limited to those listed on its packaging.
The notice also says dapoxetine is not approved by the U.S. FDA, so its safety and efficacy have not been established by the agency. It describes dapoxetine as belonging chemically to the selective serotonin reuptake inhibitor (SSRI) class and cites an increased risk of suicidal thinking and behavior among children, adolescents and young adults associated with consumption. The announcement does not provide details about the amount of any ingredient found in the capsules.
Products Worth Considering
Fitbit Versa 2 Health and Fitness Smartwatch with Bonus Bands
Blueair Blue Pure 511i Max Air Purifier for Home and Bedroom
Oura Ring 4 Smart Ring – Silver – Size 8
As an affiliate, we earn on qualifying purchases.
Recall Covers Two Product Formats
Ultimate Forza was marketed as a male performance dietary supplement. The recall is not limited to one package configuration: it applies to all lots of both the multi-capsule box and single-capsule pack identified in the notice. Consumers can check the item numbers and UPCs against the announcement to help determine whether a product is included.
The distribution period listed in the company announcement runs from 2017 through October 1, 2026, but the products were sold only through certain independently owned and operated GNC franchise locations. The notice specifically distinguishes those franchise locations from GNC corporate stores. It does not identify individual franchise locations or provide a lot-by-lot list in the supplied announcement.
The recall was initiated after testing by a third party for GNC identified the undeclared substances, according to Tonight We Ride. The company says affected stock was quarantined and sales stopped. The FDA published the company’s announcement on October 24; the agency’s posting is not an independent endorsement or, by itself, a statement that FDA tested the product.
“The company is “voluntarily recalling all lots of Ultimate Forza Male Supplement capsules to the consumer level.””
— Tonight We Ride, LLC, in the recall announcement
Ingredient Amounts and Exposure Unknown
The announcement does not state how much sildenafil, tadalafil or dapoxetine was found in the capsules, whether amounts varied among lots, or how the substances entered the product. It also does not name the independently operated franchise locations that carried the supplement. The distribution dates provide a broad period, but the notice does not give purchase totals or the number of units sold.
Although the company reported no adverse events or complaints at the time of its announcement, the notice does not establish how many consumers may have used the product or whether any later reports will be received. Consumers who believe they experienced a problem are advised to contact a health care provider and can report adverse reactions or quality concerns to the FDA’s MedWatch program.
Return Products and Report Problems
Consumers should stop taking the capsules and return any 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 loyalty account used for the purchase so the transaction can be verified. The company lists GNC Customer Service at 1-877-462-4700 and GNCRecalls@gnc-hq.com for questions.
Anyone who has had a health problem they believe may be related to the supplement should contact a physician or health care provider. The FDA says adverse reactions and product-quality problems may also be reported through MedWatch, online at www.fda.gov/medwatch/report.htm, by fax at 1-800-FDA-0178, or by mail using a report form available through the FDA. The company announcement does not give a deadline for returns or state whether further product testing or agency action is expected.
Key Questions
Which Ultimate Forza products are included in the recall?
The recall covers all lots of the Ultimate Forza Multi-Capsule/Box, item No. 810208 and UPC 868592000002, and the Ultimate Forza Single Pack, item No. 810222 and 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 products were not sold through GNC corporate stores.
What should consumers do with the product?
Stop using it immediately. Unopened or partially used product may be returned to a GNC store for a full refund. A receipt or the contact information tied to the loyalty account used for the purchase can help verify the transaction.
Why were the ingredients not listed considered a concern?
The notice says sildenafil and tadalafil may interact with nitrates in some prescription medicines and dangerously lower blood pressure. It also says dapoxetine is not FDA-approved and its safety and efficacy have not been established. People with concerns about exposure should contact a health care provider.
How can consumers ask questions or report a reaction?
For recall questions, contact GNC Customer Service at 1-877-462-4700 or GNCRecalls@gnc-hq.com. Health problems should be discussed with a physician or health care provider and may also be reported to the FDA through its MedWatch program.
Source: primary
