Natures Supplement recalls Enhanced Vegetal Vigra 200 mg Capsules, 8 count bottles, Manufacturer: Hand-shaking (Int'l) Cop. USA, ADD: Hand-shaking
Natures Supplement recalls Enhanced Vegetal Vigra 200mg capsules due to FDA finding they contain sildenafil, a drug not approved for use in supplements.
Recall notice
Marketed without an Approved NDA/ANDA; FDA analysis found product to be tainted with Sildenafil.
Contact the company & request your remedy
What happened, in plain English
Natures Supplement is recalling Enhanced Vegetal Vigra 200mg capsules because the FDA found they contain sildenafil, a drug that should not be in supplements. This poses a risk of unintended medication effects for users. Read more at govinfonow.com/recall/41243-natures-supplement-enhanced-vegetal-vigra-capsules-tainted-with-sildenafil.
Source Summary by GovInfoNow · govinfonow.com/recall/41243-natures-supplement-enhanced-vegetal-vigra-capsules-tainted-with-sildenafil · Updated October 7, 2026 · FDA enforcement record: FDA #D-0149-2018
Cite this page
“Natures Supplement Enhanced Vegetal Vigra Capsules Tainted with Sildenafil.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/41243-natures-supplement-enhanced-vegetal-vigra-capsules-tainted-with-sildenafil. Based on FDA recall #D-0149-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0149-2018%22&limit=1).
Why it’s dangerous
The capsules contain sildenafil, a medication approved for treating erectile dysfunction, which was found in the product by FDA analysis. This means users could experience unintended side effects from the drug.
Who’s affected
Anyone who purchased Enhanced Vegetal Vigra 200mg capsules from Natures Supplement. People taking medications that interact with sildenafil are at higher risk.
How to tell if you have this one
Check for the product name 'Enhanced Vegetal Vigra 200 mg Capsules, 8 count bottles' with UPC# 8931028556885. All lots produced before February 23, 2020 are affected.
- Brand
Natures Supplement- Product
Enhanced Vegetal Vigra 200 mg Capsules, 8 count bottles, Manufacturer: Hand-shaking (Int'l) Cop. USA, ADD: Hand-shaking- Category
Drug
What to do — step by step
Check Product Details
Look for the UPC number 8931028556885 on the product label.
Questions people ask
Why is this product being recalled?
The FDA found sildenafil in the product, which is a medication not approved for use in supplements.
What should I do if I have this product?
The recall record does not specify a remedy, so contact Natures Supplement directly for guidance.
Is this product safe to use?
No, the product contains sildenafil which can cause unintended side effects.
Contact Natures Supplement
We’ve drafted a message you can send Natures Supplement to request your refund or repair — edit it as you like.
Subject: Recall D-0149-2018 — Natures Supplement Enhanced Vegetal Vigra 200 mg Capsules, 8 count bottles, Manufacturer: Hand-shak Hello, I own a Enhanced Vegetal Vigra 200 mg Capsules, 8 count bottles, Manufacturer: Hand-shaking (Int'l) Cop. USA, ADD: Hand-shaking that is covered by recall D-0149-2018 from Natures Supplement. 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-0149-2018 (September 20, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0149-2018 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.