FDAClass IFebruary 24, 2016

Rhino 7 3000 recall

Rhino 7 3000, 6 count bottles, Distributed by Rhino 7, Made in USA.

Why was Rhino 7 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 3000, 6 count bottles, Distributed by Rhino 7, Made in USA.
Recalling firm
MSNV, Inc dba National Video Supply
Quantity
868 Bottles
Distribution
Nationwide
Recall date
February 24, 2016
Classification
Class I
Status
Terminated
Agency
FDA (drug)
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