Nuri Trading LLC recalls Shogun-X 7000 capsule, packaged in a) 1-count blister card and b) 10-count box, Nuri Trading LLC
Nuri Trading LLC recalls Shogun-X 7000 capsules due to undeclared tadalafil and sildenafil, unapproved drugs with unknown safety. All lots within expiry date.
Recall notice
Marketed Without An Approved NDA/ANDA: Product found to be tainted with undeclared tadalafil and sildenafil, two FDA approved drugs making them unapproved drugs for which the safety and efficacy have not been established and therefore subject to recall.
Contact the company & request your remedy
What happened, in plain English
Nuri Trading LLC is recalling Shogun-X 7000 capsules because they contain undeclared tadalafil and sildenafil, which are FDA-approved drugs but not approved for this product. This makes the capsules unapproved and potentially unsafe. Read more at govinfonow.com/recall/36233-shogun-x-7000-capsule-recall-unapproved-drugs-found.
Source Summary by GovInfoNow · govinfonow.com/recall/36233-shogun-x-7000-capsule-recall-unapproved-drugs-found · Updated October 4, 2026 · FDA enforcement record: FDA #D-0685-2021
Cite this page
“Shogun-X 7000 Capsule Recall: Unapproved Drugs Found.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/36233-shogun-x-7000-capsule-recall-unapproved-drugs-found. Based on FDA recall #D-0685-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0685-2021%22&limit=1).
Why it’s dangerous
The capsules were found to contain undeclared tadalafil and sildenafil, which are FDA-approved drugs but not approved for this product. This means the safety and effectiveness of these drugs in this product have not been established, potentially causing health risks.
Who’s affected
Anyone who owns or uses Shogun-X 7000 capsules from Nuri Trading LLC. People most at risk are those who have taken the capsules without knowing they contain unapproved drugs.
How to tell if you have this one
Check for Shogun-X 7000 capsules in 1-count blister cards or 10-count boxes from Nuri Trading LLC. All lots within expiry date.
- Brand
Nuri Trading LLC- 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 I- Status
Ongoing- Distribution
USA Nationwide
| Recall number | Product, codes & lots |
|---|---|
| D-0685-2021 | Shogun-X 7000 capsule, packaged in a) 1-count blister card and b) 10-count box, Nuri Trading LLC; all lots within expiry |
| D-0686-2021 | Thumbs Up 7 Black 25K capsule, packaged in a) 1-count blister card and b) 10-count box, Nuri Trading LLC; all lots within expiry |
| D-0687-2021 | Thumbs Up 7 White 11K capsule, packaged in a) 1-count blister card and b) 10-count box, Nuri Trading LLC; all lots within expiry |
| D-0688-2021 | 69MODE Blue 69 capsule, packaged in 10-count box, Nuri Trading LLC; all lots within expiry |
What to do — step by step
Check Product
Look for Shogun-X 7000 capsules in 1-count blister cards or 10-count boxes from Nuri Trading LLC.
Questions people ask
Why is this product being recalled?
The capsules contain undeclared tadalafil and sildenafil, which are FDA-approved drugs but not approved for this product, making them unapproved and potentially unsafe.
Are there any safety risks?
The safety and effectiveness of these drugs in this product have not been established, so there could be health risks.
What should I do if I have this product?
The recall record does not specify a remedy, so check the product and contact the manufacturer for further instructions.
Contact Nuri Trading LLC
We’ve drafted a message you can send Nuri Trading LLC to request your refund or repair — edit it as you like.
Subject: Recall D-0685-2021 — Nuri Trading LLC Nuri Trading LLC Hello, I own a Nuri Trading LLC that is covered by recall D-0685-2021 from Nuri Trading LLC. 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-0685-2021 (March 29, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0685-2021 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.