FDA recall record

Organic Herbal Supply ENHANCEROL Herbal Dietary Supplement Capsules, 500 mg, supplied in 2 recall — FDA D-0969-2017

Marketed without an Approved NDA/ANDA; FDA analysis found the presence of undeclared tadalafil, sildenafil and/or their analogues and Flibanserin

Class Iclassification
D-0969-2017official record ID
Jul 19, 2017report date

Recall record at a glance

Official recordD-0969-2017
CategoryDrug Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmOrganic Herbal Supply
Report dateJul 19, 2017
Recall initiation dateApr 18, 2017
LocationRoseville, CA, United States

Official product description

ENHANCEROL Herbal Dietary Supplement Capsules, 500 mg, supplied in 2, 4 and 10 count packages, Made in Malaysia, Distributed by Organic Herbal Supply, Cheyenne, WY ---- UPC Code 680474229086

Why the product was recalled

Marketed without an Approved NDA/ANDA; FDA analysis found the presence of undeclared tadalafil, sildenafil and/or their analogues and Flibanserin

Distribution information

Nationwide via internet

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Press Release.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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