Ultimate Forza capsules recalled over undeclared drug ingredients
Company notice identifies two packs sold through certain GNC franchises; quantities remain unspecified.
Original-source briefing · AI-written · Edited by Codex
Source event: 2026-10-24. Published: 2026-10-25T08:15:54.781Z. Updated: 2026-10-25T08:15:54.781Z.
What happened
Primary-source statement · Tonight We Ride, LLC recalled all lots of Ultimate Forza capsules on October 24 after GNC’s third-party testing found undeclared sildenafil, tadalafil and dapoxetine, according to its FDA-hosted notice. It names a ten-capsule box, item 810208 (UPC 868592000002), and single pack, item 810222 (UPC 868592000040). Distribution ran from 2017 through October 1, 2026, through certain independently owned U.S. GNC franchises, excluding corporate stores. The company instructs purchasers to stop use and return remaining product for a refund. [U.S. Food and Drug Administration, company-announcement host]
Why it matters
Primary-source statement · Health Canada’s separate guidance warns that sildenafil and tadalafil can interact with nitrate medicines such as nitroglycerin and cause potentially life-threatening low blood pressure. It says prescription-drug products need supervision by a health-care provider and that unauthorized enhancement products may not match their labels. This is general guidance dated June 10, 2021, not a Canadian finding about Ultimate Forza. The recall’s ingredient account remains the company’s report of GNC testing; the Canadian page does not independently verify that result. [Health Canada, Government of Canada] [U.S. Food and Drug Administration, company-announcement host]
What remains unknown
Evidence limits · The company reported no adverse events or complaints as of its announcement; that dated statement does not establish that nobody was harmed. The notice does not quantify capsules sold or people exposed, and does not include the underlying laboratory report. FDA hosts the announcement as a public service, rather than endorsing the product or company. [U.S. Food and Drug Administration, company-announcement host]
Recall reporting and general regulator guidance, not individual medical advice. No independent ICU laboratory test, clinician review or Canadian product-recall finding is claimed.
Read the infographic as text
TEN-CAPSULE BOX. Item 810208 · UPC 868592000002
SINGLE PACK. Item 810222 · UPC 868592000040
SCOPE. All lots · certain U.S. GNC franchises
SALES WINDOW. 2017–October 1, 2026. Corporate stores excluded.
COMPANY INSTRUCTION. Stop use; return remaining product for a refund.
Evidence limit. Company notice and identifiers. No independent ICU product test or verified total sold.
Graphic sources: U.S. Food and Drug Administration, company-announcement host
The developing record.
Earlier entries preserve what was published at that time; later entries may revise them.
2026-10-25T08:15:54.781Z · Initial report on the company’s all-lots recall, exact two-pack identifiers and franchise-only distribution, with separately attributed general drug-interaction guidance. No independent product testing or current no-harm conclusion is claimed.
Ultimate Forza capsules recalled over undeclared drug ingredients
Company notice identifies two packs sold through certain GNC franchises; quantities remain unspecified.
What happened
Tonight We Ride, LLC recalled all lots of Ultimate Forza capsules on October 24 after GNC’s third-party testing found undeclared sildenafil, tadalafil and dapoxetine, according to its FDA-hosted notice. It names a ten-capsule box, item 810208 (UPC 868592000002), and single pack, item 810222 (UPC 868592000040). Distribution ran from 2017 through October 1, 2026, through certain independently owned U.S. GNC franchises, excluding corporate stores. The company instructs purchasers to stop use and return remaining product for a refund. [U.S. Food and Drug Administration, company-announcement host]
Why it matters
Health Canada’s separate guidance warns that sildenafil and tadalafil can interact with nitrate medicines such as nitroglycerin and cause potentially life-threatening low blood pressure. It says prescription-drug products need supervision by a health-care provider and that unauthorized enhancement products may not match their labels. This is general guidance dated June 10, 2021, not a Canadian finding about Ultimate Forza. The recall’s ingredient account remains the company’s report of GNC testing; the Canadian page does not independently verify that result. [Health Canada, Government of Canada] [U.S. Food and Drug Administration, company-announcement host]
What remains unknown
The company reported no adverse events or complaints as of its announcement; that dated statement does not establish that nobody was harmed. The notice does not quantify capsules sold or people exposed, and does not include the underlying laboratory report. FDA hosts the announcement as a public service, rather than endorsing the product or company. [U.S. Food and Drug Administration, company-announcement host]
Read the infographic as text
TEN-CAPSULE BOX. Item 810208 · UPC 868592000002
SINGLE PACK. Item 810222 · UPC 868592000040
SCOPE. All lots · certain U.S. GNC franchises
SALES WINDOW. 2017–October 1, 2026. Corporate stores excluded.
COMPANY INSTRUCTION. Stop use; return remaining product for a refund.
Evidence limit. Company notice and identifiers. No independent ICU product test or verified total sold.
Graphic sources: U.S. Food and Drug Administration, company-announcement host
Original sources
Ultimate Forza company recall, October 24 · Issuer: Tonight We Ride, LLC; GNC testing described in the company notice · 2026-10-24
Health Canada: sexual-enhancement product safety · Issuer: Health Canada · 2021-06-10
Corrections
No corrections recorded.