AMA Wholesale Rhino 69 Extreme 50000: Unapproved Drug Recall
FDA recalls AMA Wholesale's Rhino 69 Extreme 50000 capsules due to undeclared tadalafil. This unapproved drug lacks safety and efficacy data. Consumers should stop using immediately.
Stop using this now
Marketed Without An Approved NDA/ANDA: FDA analysis found the product to contain undeclared tadalafil. The presence of tadalafil makes Rhino Extreme 50000 an unapproved drug for which safety and efficacy have not been established and, therefore, subject to recall.
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What happened, in plain English
AMA Wholesale is recalling Rhino 69 Extreme 50000 capsules because they contain undeclared tadalafil, an unapproved drug with no established safety or effectiveness. Using these capsules poses a risk of serious health issues due to the lack of FDA approval. Read more at govinfonow.com/recall/40617-ama-wholesale-rhino-69-extreme-50000-unapproved-drug-recall.
Source Summary by GovInfoNow · govinfonow.com/recall/40617-ama-wholesale-rhino-69-extreme-50000-unapproved-drug-recall · Updated October 7, 2026 · FDA enforcement record: FDA #D-0821-2018
Cite this page
“AMA Wholesale Rhino 69 Extreme 50000: Unapproved Drug Recall.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/40617-ama-wholesale-rhino-69-extreme-50000-unapproved-drug-recall. Based on FDA recall #D-0821-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0821-2018%22&limit=1).
Why it’s dangerous
The product contains undeclared tadalafil, which is an unapproved drug. The FDA found this substance in the product, meaning it has not been tested for safety or effectiveness. This poses a risk of serious health issues when used without proper medical oversight.
Who’s affected
Anyone who purchased Rhino 69 Extreme 50000 capsules from AMA Wholesale. People using these products for medical purposes are at highest risk due to the unapproved drug content.
How to tell if you have this one
Check for Rhino 69 Extreme 50000 capsules in 1 per blister pack. The product was distributed by AMA Wholesale Inc. in Chino Hills, CA, with UPC code 718122071128. All lots are affected.
- Brand
AMA Wholesale- Product
Rhino 69 Extreme 50000 packaged in 1 capsule per blister pack, Distributed by AMA Wholesale Inc. Chino Hills, CA- Category
Drug
What to do — step by step
Stop Using Now
Immediately stop using Rhino 69 Extreme 50000 capsules as they contain undeclared tadalafil, an unapproved drug with no established safety or effectiveness.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide within the US” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 3 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-0821-2018 (April 12, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0821-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 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.