CLASS I Drug recall · Reported 10 Jan 2018 · FDA Enforcement Report
Enhanced Vegetal Vigra, Manufacturer: Hand-shaking (Int'l) Cop recalled
Natures Supplement is recalling Enhanced Vegetal Vigra, Manufacturer: Hand-shaking (Int'l) Cop, distributed in Florida. The recall was initiated on 20 Sep 2017 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-0149-2018
- FDA event ID
- 78073
- Recalling firm
- Natures Supplement, Lake Worth, FL
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 20 Sep 2017
- FDA classified
- 4 Jan 2018
- Reported
- 10 Jan 2018
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Hidden Drug Ingredients
Timeline
| 20 Sep 2017 | Recall initiated by company | |
| 4 Jan 2018 | Classified by FDA | +106 days |
| 10 Jan 2018 | Published in enforcement report | +6 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 product to be tainted with Sildenafil.
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
Enhanced Vegetal Vigra 200 mg Capsules, 8 count bottles, Manufacturer: Hand-shaking (Int'l) Cop. USA, ADD: Hand-shaking Mansion, the 5th Ave., Stanford, USA --- UPC# 8931028556885
Where it was distributed
Florida
Questions about this recall
Why was it recalled?
Marketed without an Approved NDA/ANDA; FDA analysis found product to be tainted with Sildenafil.
Which lots are affected?
All lots, Exp. 02/23/2020
Where was it sold?
Florida
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.