Rhino 7 Platinum 3000 recall
Rhino 7 Platinum 3000, 1 count Blister Pack, Distributed by Rhino 7, Made in USA
Why was Rhino 7 Platinum 3000 recalled?
Marketed without an Approved NDA/ANDA: Products contain undeclared active pharmaceutical ingredients; desmethyl carbondenafil and dapoxetine.
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?
All lots
- Product
- Rhino 7 Platinum 3000, 1 count Blister Pack, Distributed by Rhino 7, Made in USA
- Recalling firm
- Premiere Sales Group
- Distribution
- Nationwide
- Recall date
- February 24, 2016
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)