The Recall Desk
CriticalFDA (Drugs)·D-0671-2016·Announced 2016-02-24

Rhino 7 Platinum 3000 Recalled for Undeclared Active Ingredients

MSNV, Inc dba National Video Supply is recalling Rhino 7 Platinum 3000 single blister packs because they contain undeclared active pharmaceutical ingredients.

What this means for you

Highest-severity recall. Risk of serious injury or death is documented or strongly suspected. Stop using the product now and follow the agency's instructions.

Our severity reasoning: The agency classification is FDA Class I, which mandates a severity score of 5 according to the rubric.

Plain-English summary

MSNV, Inc dba National Video Supply is recalling Rhino 7 Platinum 3000, Single Blister Packs. The product was distributed nationwide. The recall involves 460 blister packs across all lots.

The FDA is recalling this product because it was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA). The products contain undeclared active pharmaceutical ingredients, specifically desmethyl carbondenafil and dapoxetine.

Consumers who have purchased Rhino 7 Platinum 3000 should stop using the product and contact the recalling firm for further instructions.

The recalled product

Product
Rhino 7 Platinum 3000, Single Blister Packs, distributed By Rhino 7, Made in USA
Affected units
460

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • All Lots

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 2 recalled by MSNV, Inc dba National Video Supply under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 2 products in this recall →

Same manufacturer · MSNV, Inc dba National Video Supply

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