vitaliKOR Ready When You Are recall
vitaliKOR Ready When You Are, Fast Acting Formula Dietary Supplement capsules, 40 count bottle, Distributed by Vitality Research Labs, LLC, Las Vegas, NV 89148.
Why was vitaliKOR Ready When You Are recalled?
Marketed Without an Approved NDA/ANDA: FDA sampling found undeclared vardenafil and tadalafil in vitaliKOR capsules
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
LOT K58Q Exp 01/16 LOT F50Q Exp 07/16
- Product
- 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
- Quantity
- 11,523 bottles of lot K58Q; 54,255 bottles of lot F50Q
- Distribution
- Nationwide
- Recall date
- June 18, 2014
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)