Super Samurai-X Recall: Undeclared Sildenafil in Supplements
SOS Telecom Inc. recalls Super Samurai-X dietary supplements due to undeclared sildenafil. Lot 7920499, best use by 10/15/2016.
Stop using this now
Marketed without an approved NDA/ANDA: FDA sample analyses revealed the presence of undeclared sildenafil and/or its analogs in products marketed as dietary supplements
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What happened, in plain English
SOS Telecom Inc. is recalling Super Samurai-X, a dietary supplement marketed as containing 1000 mg per capsule. The FDA found that the product was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA) and contained undeclared sildenafil or its analogs. This means the product contains a prescription drug ingredient not listed on the label. Read more at govinfonow.com/recall/42758-super-samurai-x-recall-undeclared-sildenafil-in-supplements.
Source Summary by GovInfoNow · govinfonow.com/recall/42758-super-samurai-x-recall-undeclared-sildenafil-in-supplements · Updated October 9, 2026 · FDA enforcement record: FDA #D-0104-2017
Cite this page
“Super Samurai-X Recall: Undeclared Sildenafil in Supplements.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/42758-super-samurai-x-recall-undeclared-sildenafil-in-supplements. Based on FDA recall #D-0104-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0104-2017%22&limit=1).
Why it’s dangerous
The product contains undeclared sildenafil, a prescription medication used to treat erectile dysfunction, which is not allowed in dietary supplements. Taking undeclared sildenafil can cause dangerous interactions with other medications, such as nitrates, leading to sudden drops in blood pressure and potentially serious health consequences.
Who’s affected
Consumers who purchased Super Samurai-X dietary supplements, specifically those with Lot number 7920499 and a best use date of 10/15/2016. Individuals in New York are noted as part of the distribution pattern.
How to tell if you have this one
Check your product for the name 'Super Samurai-X', dosage '1000 mg', packaging of '1 capsule per pack' with '24 single packs per box'. Look specifically for Lot number 7920499 and a best use date of 10/15/2016.
- Brand
Super Samurai-X- 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
Terminated- Distribution
NY
| Recall number | Product, codes & lots |
|---|---|
| D-0101-2017 | Tiger-X, 1200 mg, 1 capsule per pack , 24 single packs per box; Lot No: 9236999; Best use by: 12/16/2016 |
| D-0102-2017 | Ninja-X, 4200 mg, 1 capsule per pack, 24 single packs per box.; Lot: 7920888; Best Use by: 6/31/2018 |
| D-0103-2017 | Ginseng Power-X , 1800 mg, 1 capsule per pack , 24 single packs per box.; Lot: 7788965; Best use by: 10/15/2018 |
| D-0104-2017 | Super Samurai-X , 1000 mg, 1 capsule per pack , 24 single packs per box.; Lot: 7920499; Best use by: 10/15/2016 |
What to do — step by step
Stop using the product
Do not consume any capsules from the recalled Super Samurai-X boxes.
Dispose of the product
Discard the product safely to prevent accidental ingestion by others.
Where it went and when
Where it was distributed
Distributed in New York.
FDA distribution: “NY” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: New York.
Recall timeline
FDA terminated this recall 2.1 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-0104-2017 (May 12, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0104-2017 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 9, 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.