RecallRadar
FDA · DrugsClass I

EnShiShiXiangNiShangMaoYouXianGongSi drug recall: Endurance Boost With Horny Goat Weed

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Drugs
Classification
Class I
Status
Ongoing
Event ID
96833
Recall initiated
May 6, 2025
Classified by FDA
May 29, 2025
Posted in Enforcement Report
Jun 4, 2025
Recalling firm
EnShiShiXiangNiShangMaoYouXianGongSi
Firm location
Unknown, China
Initiated by
Voluntary: Firm initiated
Firm notified customers by
Press Release
Products in this event
1

What to do

Compare the product, lot or serial numbers below with what you have. If you use a prescription drug or medical device in this recall, talk to your pharmacist or health care provider before you stop using it, and follow the firm's instructions.

View the official FDA record ↗

Reason for recall

Marketed without approved NDA/ANDA: The product has been found to be tainted with Sildenafil and Propoxyphenylsildenafil (a sildenafil analogue).

What the classification means

  • Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.

About this recall

The firm started this recall on May 6, 2025. FDA classified it 23 days later, on May 29, 2025. Distribution reported by FDA: Nationwide Via Amazon Platform

Recalled products (1)

  • D-0453-2025 Class I Ongoing

    ENDURANCE BOOST WITH HORNY GOAT WEED, 500mg, 20 capsules per carton, VEPEMVA Nutrition Supplement....rgy and Endurance, UPC X004BB9Z8N

    Codes / lots: Lot: 250214PRO, Expiration Date: 02/14/2027.

    Quantity: 600, 20-count cartons

Source and freshness

Source
U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA drug enforcement dataset
Official notice
FDA Enforcement Report, event 96833
Raw record
openFDA API (JSON)
Dataset last updated by FDA
Nov 3, 2026
Imported by RecallRadar
Nov 4, 2026

Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.