US Drug Recall Register
Class I · High risk Terminated Initiated Sep 15, 2017 (9 years ago)

RHINO 7 Platinum 5000, capsule, Proprietary Material: 750mg, 1-capsule packets…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical Ingredients sildenafil, desmethyl carbodenafil and tadalafil.

What was recalled

RHINO 7 Platinum 5000, capsule, Proprietary Material: 750mg, 1-capsule packets, distributed by Fifty Shades Bayside, NY 11361, UPC 617135861224

Recalling firm
Gadget Island, Inc
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0103-2018

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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