Rhino 7 3000 Recall: Undeclared Drug Ingredients
Tf Supplements recalls RHINO 7 3000 bottles due to undeclared desmethyl carbondenafil and dapoxetine. Check your bottle immediately.
Stop using this now
Marketed without an Approved NDA/ANDA: Products contain undeclared desmethyl carbondenafil and dapoxetine.
Contact the company
What happened, in plain English
Tf Supplements is recalling all lots of the RHINO 7 3000 supplement because it contains undeclared prescription drug ingredients: desmethyl carbondenafil and dapoxetine. These substances are not listed on the label, which poses a risk to consumers who may have allergies or medical conditions that interact with these drugs. The product was distributed nationwide in 6-count bottles. Read more at govinfonow.com/recall/43616-tf-supplements-recalls-rhino-7-3000-6-count-bottle-distributed.
Source Summary by GovInfoNow · govinfonow.com/recall/43616-tf-supplements-recalls-rhino-7-3000-6-count-bottle-distributed · Updated October 12, 2026 · FDA enforcement record: FDA #D-0771-2016
Cite this page
“Rhino 7 3000 Recall: Undeclared Drug Ingredients.” GovInfoNow, updated October 12, 2026. https://govinfonow.com/recall/43616-tf-supplements-recalls-rhino-7-3000-6-count-bottle-distributed. Based on FDA recall #D-0771-2016 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0771-2016%22&limit=1).
Why it’s dangerous
The product contains undeclared desmethyl carbondenafil and dapoxetine, which are active pharmaceutical ingredients not approved for use in this type of supplement without an NDA/ANDA. Taking these undisclosed drugs can lead to serious health interactions or adverse effects that the consumer is unaware they are ingesting.
Who’s affected
Consumers who purchased the RHINO 7 3000 supplement, specifically those who bought the 6-count bottle distributed by Rhino 7. Individuals with heart conditions, low blood pressure, or allergies to the undeclared ingredients are at particular risk.
How to tell if you have this one
Look for a bottle labeled "RHINO 7 3000" with a count of 6, distributed by Rhino 7 and marked as Made in USA. The recall covers all lots of this product.
- Brand
Rhino 7- Category
Drug
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class I- Status
Terminated- Distribution
Nationwide
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-0771-2016 | RHINO 7 3000, 6 count Bottle, Distributed by Rhino 7, Made in USA; All lots | 350 Bottles |
| D-0772-2016 | Rhino 7 Platinum 3000, 1 count Blister Pack, Distributed by Rhino 7, Made in USA, UPC 700729253748; All lots | 128 Blister Packs |
What to do — step by step
Stop using the supplement
Do not consume any more of the RHINO 7 3000 product due to the presence of undeclared drug ingredients.
Discard or return the product
The record does not specify a return address or refund process, so you should dispose of the remaining bottles safely.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 6.6 years after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
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-0771-2016 (September 25, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0771-2016 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 12, 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.