US Drug Recall Register
Class I · High risk Terminated Initiated Apr 18, 2017 (9 years ago)

ZRECT for Women Herbal Dietary Supplement Capsules, 500 mg, supplied in 30 count…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

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

What was recalled

ZRECT for Women Herbal Dietary Supplement Capsules, 500 mg, supplied in 30 count packages, Distributed by Organic Herbal Supply, Roseville, CA --- UPC Code 680474229055

Recalling firm
Organic Herbal Supply
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0970-2017

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.