US Drug Recall Register
Class I · High risk Terminated Initiated Nov 19, 2013 (13 years ago)

vitaliKOR Ready When You Are, Fast Acting Formula Dietary Supplement capsules, 40 count…

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

Why it was recalled

Marketed Without an Approved NDA/ANDA: FDA sampling found undeclared vardenafil and tadalafil in vitaliKOR capsules

What was recalled

vitaliKOR Ready When You Are, Fast Acting Formula Dietary Supplement capsules, 40 count bottle, Distributed by Vitality Research Labs, LLC, Las Vegas, NV 89148.

Recalling firm
Vitality Research Labs LLC
Origin
NV, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1364-2014

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.