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

ZDaily Daily Testosterone and Llibido Booster Herbal Dietary Supplement Capsules, 500 mg…

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

ZDaily Daily Testosterone and Llibido Booster Herbal Dietary Supplement Capsules, 500 mg, supplied in 2, 4 and 10 count packages, Distributed by Organic Herbal Supply, Roseville, CA --- UPC Code 680474229062

Recalling firm
Organic Herbal Supply
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0967-2017

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.

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