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