CLASS I ONGOING Drug recall · Reported 6 Sep 2023 · FDA Enforcement Report
Vegetal Vigra, 200mg capsules, Manufacturer: Hand-shaking recalled
APG Seven is recalling Vegetal Vigra, 200mg capsules, Manufacturer: Hand-shaking (Int'l) Corp, distributed nationwide in the US. The recall was initiated on 3 Aug 2023 and the FDA has classified it as Class I.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-1150-2023
- FDA event ID
- 92892
- Recalling firm
- APG Seven, Miami, FL
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- 3 Aug 2023
- FDA classified
- 15 Sep 2023
- Reported
- 6 Sep 2023
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Hidden Drug Ingredients
Timeline
| 3 Aug 2023 | Recall initiated by company | |
| 6 Sep 2023 | Published in enforcement report | +34 days |
| 15 Sep 2023 | Classified by FDA | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
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.
Products marketed as supplements sometimes contain undeclared prescription drug ingredients such as sildenafil or sibutramine. These can interact dangerously with other medicines.
Product as listed by the FDA
Vegetal Vigra, 200mg capsules, 8-count bottle, Manufacturer: Hand-shaking (Int'l) Corp. USA ADD: Hand-shaking Mansion, the 5th Ave., Stanford, USA. UPC 8 931028 556885
Where it was distributed
Nationwide in the USA
Questions about this recall
Why was it recalled?
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.
Which lots are affected?
All lots, Expires: 01/31/2025
Where was it sold?
Nationwide in the USA
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.