Rhino 7 3000 Recall: Undeclared Drug Ingredients
Premiere Sales Group recalls Rhino 7 3000 bottles due to undeclared active pharmaceutical ingredients. Check your bottle lot.
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
Premiere Sales Group is recalling all lots of Rhino 7 3000, a 6-count bottle distributed by Rhino 7 and made in the USA. The product was marketed without an approved New Drug Application or Abbreviated New Drug Application because it contains undeclared active pharmaceutical ingredients: desmethyl carbondenafil and dapoxetine. This means consumers are taking substances not listed on the label. Read more at govinfonow.com/recall/43609-premiere-sales-group-recalls-rhino-7-3000-6-count-bottle.
Source Summary by GovInfoNow · govinfonow.com/recall/43609-premiere-sales-group-recalls-rhino-7-3000-6-count-bottle · Updated October 12, 2026 · FDA enforcement record: FDA #D-0672-2016
Cite this page
“Rhino 7 3000 Recall: Undeclared Drug Ingredients.” GovInfoNow, updated October 12, 2026. https://govinfonow.com/recall/43609-premiere-sales-group-recalls-rhino-7-3000-6-count-bottle. Based on FDA recall #D-0672-2016 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0672-2016%22&limit=1).
Why it’s dangerous
The product contains desmethyl carbondenafil and dapoxetine, which were not declared on the label. Taking undeclared active pharmaceutical ingredients can lead to unexpected side effects or interactions with other medications without the user's knowledge.
Who’s affected
Consumers who purchased Rhino 7 3000 supplements distributed nationwide. Individuals seeking sexual enhancement products are at risk of ingesting undeclared drugs.
How to tell if you have this one
Look for Rhino 7 3000 in a 6-count bottle. The product is distributed by Rhino 7, made in the USA, and includes all lots. It was sold nationwide.
- 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-0672-2016 | Rhino 7 3000, 6 count Bottle, Distributed by Rhino 7, Made in USA; All lots | 337 bottles |
| D-0673-2016 | Rhino 7 Platinum 3000, 1 count Blister Pack, Distributed by Rhino 7, Made in USA; All lots | — |
What to do — step by step
Stop using the product
Cease consumption of any Rhino 7 3000 bottles immediately due to undeclared drug ingredients.
Discard or return the item
The record does not specify a return address or disposal method, so you should dispose of it 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 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.
Questions people ask
When was this recall announced?
The recall date listed is September 30, 2015.
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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-0672-2016 (September 30, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0672-2016 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.