QMart recalls IMPERIAL GOLD 2000, Male Sexual Performance Enhancement, 1 Capsule, UPC 718122040702
QMart recalls Imperial Gold 2000 male performance capsules due to unapproved drug ingredients. FDA found tadalafil or sildenafil without proper FDA approval.
Recall notice
Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.
Contact the company & request your remedy
What happened, in plain English
QMart is recalling Imperial Gold 2000 male sexual performance capsules because they contain unapproved drugs like tadalafil or sildenafil. This poses a health risk as these drugs require FDA approval for safety. Read more at govinfonow.com/recall/36222-qmart-imperial-gold-2000-capsules-unapproved-drug-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/36222-qmart-imperial-gold-2000-capsules-unapproved-drug-risk · Updated October 4, 2026 · FDA enforcement record: FDA #D-0368-2021
Cite this page
“QMart Imperial Gold 2000 Capsules: Unapproved Drug Risk.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/36222-qmart-imperial-gold-2000-capsules-unapproved-drug-risk. Based on FDA recall #D-0368-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0368-2021%22&limit=1).
Why it’s dangerous
The capsules contain tadalafil or sildenafil without FDA approval. These drugs are prescription medications that can cause serious health issues if misused without proper medical supervision.
Who’s affected
Anyone who purchased Imperial Gold 2000 capsules from QMart. Men using these products for sexual performance enhancement are at risk due to unapproved ingredients.
How to tell if you have this one
Check for the product name 'Imperial Gold 2000', 1 capsule, UPC 718122040702, and QMart as the manufacturer. The product is marketed for male sexual performance enhancement.
- Brand
QMart- Category
Drug
All 4 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 II- Status
Ongoing- Distribution
USA Nationwide
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-0368-2021 | IMPERIAL GOLD 2000, Male Sexual Performance Enhancement, 1 Capsule, UPC 718122040702; All | 200 boxes |
| D-0369-2021 | PremierZen Extreme 3000, Male Sexual Performance Enhancement, 1 Capsule, UPC 728175421887; All | 500 boxes |
| D-0370-2021 | Burro en Primavera, 2 capsules, UPC 638632431055; All | 500 boxes |
| D-0371-2021 | Imperial Platinum 2000, 1 capsule, UPC 718122040702; All | 200 boxes |
What to do — step by step
Check Product Details
Identify the product by checking for the UPC 718122040702 and QMart as the manufacturer.
Questions people ask
Is this product safe to use?
The FDA found unapproved drugs in this product, so it is not safe without proper medical supervision.
What should I do if I have this product?
The recall record does not specify a remedy, so contact QMart directly for guidance.
Why was this product recalled?
The FDA analysis detected tadalafil or sildenafil without FDA approval, which is illegal for over-the-counter sale.
Contact QMart
We’ve drafted a message you can send QMart to request your refund or repair — edit it as you like.
Subject: Recall D-0368-2021 — QMart QMart Hello, I own a QMart that is covered by recall D-0368-2021 from QMart. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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-0368-2021 (March 31, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0368-2021 to see it in context.
- Plain-language summary written by qwen3:4b on October 4, 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.