One Source Vitality Recall: Undeclared Sildenafil Hazard
One Source Nutrition recalls Vitality male enhancement supplements due to undeclared sildenafil and tadalafil. Check your bottle for affected lots.
Stop using this now
Marketed without an approved NDA/ANDA: Product found to be tainted with undeclared sildenafil and tadalafil.
Contact the company
What happened, in plain English
One Source Nutrition, Inc. is recalling its Vitality Fast Acting Male Enhancement Product because it contains undeclared prescription drugs sildenafil and tadalafil. These ingredients are not listed on the label and can cause dangerous health interactions or side effects. The recall covers all lots of the product distributed nationwide in the U.S.A. Read more at govinfonow.com/recall/32270-one-source-vitality-recall-undeclared-sildenafil-hazard.
Source Summary by GovInfoNow · govinfonow.com/recall/32270-one-source-vitality-recall-undeclared-sildenafil-hazard · Updated October 9, 2026 · FDA enforcement record: FDA #D-0281-2025
Cite this page
“One Source Vitality Recall: Undeclared Sildenafil Hazard.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/32270-one-source-vitality-recall-undeclared-sildenafil-hazard. Based on FDA recall #D-0281-2025 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0281-2025%22&limit=1).
Why it’s dangerous
The product is tainted with undeclared sildenafil and tadalafil, which are prescription drugs used to treat erectile dysfunction and pulmonary hypertension. Taking these undeclared ingredients can lead to serious health risks, including dangerously low blood pressure, especially if combined with other medications or underlying heart conditions.
Who’s affected
Consumers who purchased the Vitality Fast Acting Male Enhancement Product, available in one-capsule packets or six-capsule bottles, are at risk. Individuals taking other medications, particularly nitrates for chest pain, are especially vulnerable to severe adverse reactions.
How to tell if you have this one
Look for the brand name 'One Source Nutrition' and the product name 'Vitality, Fast Acting Male Enhancement Product'. It may be sold as a dietary supplement in either one capsule per packet or six capsules per bottle formats. The record states that all lots are affected and were distributed nationwide in the U.S.A.
- Brand
One Source Nutrition- Category
Drug
What to do — step by step
Stop taking the product immediately
Do not consume any more of the Vitality supplement due to the risk of undeclared prescription drugs.
Discard or return the product
The recall record does not specify a return address or refund process, so dispose of the product safely.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide in the U.S.A” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 34 days after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0281-2025 (February 20, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0281-2025 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 9, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.