FDAClass IMarch 16, 2016

Rhino 7 Platinum 3000 recall

Rhino 7 Platinum 3000, 1 count Blister Pack, Distributed by Rhino 7, Made in USA, UPC 700729253748

Why was Rhino 7 Platinum 3000 recalled?

Marketed without an Approved NDA/ANDA: Products contain undeclared 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, UPC 700729253748
Recalling firm
Tf Supplements
Quantity
128 Blister Packs
Distribution
Nationwide
Recall date
March 16, 2016
Classification
Class I
Status
Terminated
Agency
FDA (drug)
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