CLASS I ONGOING Drug recall · Reported 4 Jun 2025 · FDA Enforcement Report
Endurance Boost With Horny Goat Weed, 500mg recalled
EnShiShiXiangNiShangMaoYouXianGongSi is recalling Endurance Boost With Horny Goat Weed, 500mg per, Vepemva Nutrition Supplement....rgy and, distributed nationwide in the US. The recall was initiated on 6 May 2025 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-0453-2025
- FDA event ID
- 96833
- Recalling firm
- EnShiShiXiangNiShangMaoYouXianGongSi, Unknown, N/A
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- 6 May 2025
- FDA classified
- 29 May 2025
- Reported
- 4 Jun 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Hidden Drug Ingredients
Timeline
| 6 May 2025 | Recall initiated by company | |
| 29 May 2025 | Classified by FDA | +23 days |
| 4 Jun 2025 | 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 approved NDA/ANDA: The product has been found to be tainted with Sildenafil and Propoxyphenylsildenafil (a sildenafil analogue).
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
ENDURANCE BOOST WITH HORNY GOAT WEED, 500mg, 20 capsules per carton, VEPEMVA Nutrition Supplement....rgy and Endurance, UPC X004BB9Z8N
Where it was distributed
Nationwide Via Amazon Platform
Stores named: Amazon, Online Retailers
Questions about this recall
Why was it recalled?
Marketed without approved NDA/ANDA: The product has been found to be tainted with Sildenafil and Propoxyphenylsildenafil (a sildenafil analogue).
Which lots are affected?
Lot: 250214PRO, Expiration Date: 02/14/2027.
Where was it sold?
Nationwide Via Amazon Platform
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.