RecallHawk
Class I Recall

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

EnShiShiXiangNiShangMaoYouXianGongSi

Summary

The FDA issued a Class I for ENDURANCE BOOST WITH HORNY GOAT WEED, 500mg, 20 capsules per carton, VEPEMVA Nu by EnShiShiXiangNiShangMaoYouXianGongSi. Reason: Marketed without approved NDA/ANDA: The product has been found to be tainted with Sildenafil and Propoxyphenylsildenafil (a sildenafil analogue)..

Details

Source

Drug Recall

External ID

D-0453-2025

Action Date

2025-06-04

Status

Ongoing

Category

drug

Product Description

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

Lot/Code Info: Lot: 250214PRO, Expiration Date: 02/14/2027.

Quantity Affected: 600, 20-count cartons

Reason for Recall

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

Distribution

Nationwide Via Amazon Platform

Type: Voluntary: Firm initiated

Recall Initiated: 2025-05-06

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 50 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (EnShiShiXiangNiShangMaoYouXianGongSi) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does EnShiShiXiangNiShangMaoYouXianGongSi have FDA actions?

This is the only FDA action we have on record for EnShiShiXiangNiShangMaoYouXianGongSi in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "D-0453-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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