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
- Manufacturer
- MSNV, Inc dba National Video Supply
- Category
- Drug — Unapproved Supplement
- 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 →Related recalls
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