CLASS I Drug recall · Reported 18 Jun 2014 · FDA Enforcement Report
vitaliKOR Ready When You recalled by Vitality Research Labs
Vitality Research Labs is recalling vitaliKOR Ready When You Are, Fast Acting Formula Dietary Supplement capsules, distributed nationwide in the US. The recall was initiated on 19 Nov 2013 and the FDA has classified it as Class I.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-1364-2014
- FDA event ID
- 66839
- Recalling firm
- Vitality Research Labs, Las Vegas, NV
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 19 Nov 2013
- FDA classified
- 11 Jun 2014
- Reported
- 18 Jun 2014
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Labeling Errors
Timeline
| 19 Nov 2013 | Recall initiated by company | |
| 11 Jun 2014 | Classified by FDA | +204 days |
| 18 Jun 2014 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Marketed Without an Approved NDA/ANDA: FDA sampling found undeclared vardenafil and tadalafil in vitaliKOR capsules
Product as listed by the FDA
vitaliKOR Ready When You Are, Fast Acting Formula Dietary Supplement capsules, 40 count bottle, Distributed by Vitality Research Labs, LLC, Las Vegas, NV 89148.
Where it was distributed
Nationwide
Questions about this recall
Why was it recalled?
Marketed Without an Approved NDA/ANDA: FDA sampling found undeclared vardenafil and tadalafil in vitaliKOR capsules
Which lots are affected?
LOT K58Q Exp 01/16 LOT F50Q Exp 07/16
Where was it sold?
Nationwide
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.