US Drug Recall Register
Class I · High risk Terminated Initiated Apr 9, 2019 (7 years ago)

Aphrodisiac Platinum 40000, Proprietary Raw Material 6000 mg, 1 count blister card, 24…

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

Why it was recalled

Marketed without an approved NDA/ANDA: FDA analysis has found the product to be tainted with sildenafil

What was recalled

Aphrodisiac Platinum 40000, Proprietary Raw Material 6000 mg, 1 count blister card, 24 cards per box, Distributed by: APhrodisiac. UPC Code 644118128135

Recalling firm
Select Distributions LLC
Origin
MI, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1344-2019

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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