Stop using now Drug recall · FDA · Published August 3, 2023

APG SEVEN Vegetal Vigra 200mg Capsules: Unapproved Drug Recall

APG SEVEN recalls Vegetal Vigra 200mg capsules due to FDA finding it contains unapproved sildenafil. All lots of this product are affected and should be stopped use immediately.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #D-1150-2023Drug APG SEVEN ›

Stop using this now

Marketed Without an Approved NDA/ANDA: FDA analysis found the product to be tainted with sildenafil an ingredient found in a FDA approved product for the treatment of male sexual enhancement, making this an unapproved drug.

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Contact the company

Recalling firmAPG SEVEN, INC12030 Sw 129th Ct Ste 205 · Miami, FL 33186-4584

✎ GovInfoNow plain-language explainer

APG SEVEN is recalling Vegetal Vigra 200mg capsules because the FDA found it contains sildenafil, an ingredient in approved male sexual enhancement drugs. This makes the product unapproved and potentially unsafe for use. Read more at govinfonow.com/recall/33225-apg-seven-vegetal-vigra-200mg-capsules-unapproved-drug-recall.

Source Summary by GovInfoNow · govinfonow.com/recall/33225-apg-seven-vegetal-vigra-200mg-capsules-unapproved-drug-recall · Updated August 17, 2026 · FDA enforcement record: FDA #D-1150-2023

Cite this page

“APG SEVEN Vegetal Vigra 200mg Capsules: Unapproved Drug Recall.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/33225-apg-seven-vegetal-vigra-200mg-capsules-unapproved-drug-recall. Based on FDA recall #D-1150-2023 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1150-2023%22&limit=1).

The FDA announced on August 3, 2023, that APG SEVEN, INC voluntarily recalled Vegetal Vigra capsules because the product was marketed without an approved New Drug Application or Abbreviated New Drug Application. The agency found the drug tainted with sildenafil, an ingredient in an FDA-approved treatment for male sexual enhancement.

How to tell if you have it

Brand: APG SEVEN
Product: Vegetal Vigra, 200mg capsules, 8-count bottle
Manufacturer: Hand-shaking (Int'l) Corp. USA
UPC: 8 931028 556885
Lot/Expiration: All lots, Expires: 01/31/2025
Distribution: Nationwide in the USA
Quantity: 120 bottles

The hazard

The FDA stated that Vegetal Vigra is an unapproved drug because it contains sildenafil. The agency's analysis found the product tainted with this ingredient, which is found in FDA-approved products for the treatment of male sexual enhancement.

Context

GovInfoNow's records show other recent recalls of similar products include StuffbyNainax MR 7 SUPER 700000 Capsules (2025-12-15) and Shoolin Pharma Chem Sildenafil Recall (2026-08-03). Amgen Recalls Corlanor 7.5mg Tablets Due to Foreign Substance was also reported on 2026-06-04.

How to tell if you have this one

Check for Vegetal Vigra 200mg capsules in 8-count bottles. The product was sold by APG SEVEN with UPC 8 931028 556885 and expires 01/31/2025. All lots are affected.

Brand
APG SEVEN
Product
Vegetal Vigra, 200mg capsules, 8-count bottle, Manufacturer: Hand-shaking (Int'l) Corp. USA ADD: Hand-shaking Mansion
Category
Drug

Based on the official FDA remedy

What to do — step by step

Stop Using Now
Immediately stop using Vegetal Vigra 200mg capsules as they contain unapproved sildenafil.

Where it went and when

Where it was distributed

Distributed nationwide.

FDA distribution: “Nationwide in the USA” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 34 days after the firm started it.

Aug 3, 2023Firm started the recall
Sep 6, 2023Published in FDA’s Enforcement Report
Sep 15, 2023FDA classified it Class I

Dates from the agency record only; steps without a date are left out.

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Link to this recall

<a href="https://govinfonow.com/recall/33225-apg-seven-vegetal-vigra-200mg-capsules-unapproved-drug-recall">APG SEVEN Vegetal Vigra 200mg Capsules: Unapproved Drug Recall (GovInfoNow)</a>

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-1150-2023 (August 3, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1150-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 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.