FDA Recalls Rhino 7 Platinum 30000 Capsules for Unapproved Tadafila Content
Motto International Corp is recalling Rhino 7 Platinum 30000 Capsules because FDA analysis found the product contains tadalafil, an unapproved active ingredient.
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
Motto International Corp is recalling Rhino 7 Platinum 30000 Capsules, packaged in 2, 4, and 10 count blister cards. The product was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA). FDA analysis determined that the product contains tadalafil, a drug ingredient not listed on the label.
The recall covers all lots remaining within their expiration dates. The product was distributed in Texas. Consumers who purchased this product should stop using it and contact the manufacturer or their healthcare provider for guidance.
The recalled product
- Product
- Rhino 7 Platinum 30000 Capsules, in blue,orange,black background with red,white,blue,gray text in hologram paper packaging, packaged in 2, 4, and 10 count blister cards, Motto International, Dallas, TX
- Manufacturer
- Motto International Corp
- Category
- Drug — Unapproved Supplement
- Affected units
- 5
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 remaining within expiry.
Distribution
Distributed in 1 state:
Part of a larger recall action
This product is one of 4 recalled by Motto International Corp 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 4 products in this recall →Related recalls
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