Rhino 7 3000 Recall: Undeclared Drug Ingredients
MSNV Inc recalls Rhino 7 3000 bottles due to undeclared active ingredients. Check your lot numbers and consult a doctor if consumed.
Stop using this now
Marketed without an Approved NDA/ANDA: Products contain undeclared active pharmaceutical ingredients; desmethyl carbondenafil and dapoxetine.
Contact the company
What happened, in plain English
MSNV, Inc dba National Video Supply is recalling Rhino 7 3000 supplements because they contain undeclared active pharmaceutical ingredients: desmethyl carbondenafil and dapoxetine. These products were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA). The recall covers all lots of the 6-count bottles distributed nationwide. Read more at govinfonow.com/recall/43606-msnv-inc-dba-national-video-supply-recalls-rhino-7-3000.
Source Summary by GovInfoNow · govinfonow.com/recall/43606-msnv-inc-dba-national-video-supply-recalls-rhino-7-3000 · Updated October 12, 2026 · FDA enforcement record: FDA #D-0670-2016
Cite this page
“Rhino 7 3000 Recall: Undeclared Drug Ingredients.” GovInfoNow, updated October 12, 2026. https://govinfonow.com/recall/43606-msnv-inc-dba-national-video-supply-recalls-rhino-7-3000. Based on FDA recall #D-0670-2016 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0670-2016%22&limit=1).
Why it’s dangerous
The supplement contains undeclared active pharmaceutical ingredients, specifically desmethyl carbondenafil and dapoxetine. These substances can cause serious health issues, including dangerous interactions with other medications or adverse reactions in people with certain medical conditions, without their knowledge.
Who’s affected
Consumers who purchased Rhino 7 3000 supplements from retailers across the United States. Individuals taking the product are at risk of unexpected drug interactions or side effects due to the undeclared ingredients.
How to tell if you have this one
Look for Rhino 7 3000 supplements in 6-count bottles distributed by Rhino 7 and made in the USA. The recall applies to 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-0670-2016 | Rhino 7 3000, 6 count bottles, Distributed by Rhino 7, Made in USA.; All Lots | 868 Bottles |
| D-0671-2016 | Rhino 7 Platinum 3000, Single Blister Packs, distributed By Rhino 7, Made in USA; All Lots | 460 Blister Packs |
What to do — step by step
Stop taking the supplement
Discontinue use immediately if you have purchased Rhino 7 3000 supplements.
Consult a healthcare provider
Speak with your doctor about any health concerns related to consuming the undeclared ingredients.
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 20 months 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-0670-2016 (October 1, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0670-2016 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.