PlainRecalls
FDA Drug Critical Class I Terminated

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

Reported: June 19, 2019 Initiated: April 9, 2019 #D-1344-2019

Product Description

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

Reason for Recall

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

Details

Recalling Firm
SELECT DISTRIBUTIONS LLC
Units Affected
60 boxes
Distribution
MI, OH
Location
Ferndale, MI

Frequently Asked Questions

What product was recalled?
Aphrodisiac Platinum 40000, Proprietary Raw Material 6000 mg, 1 count blister card, 24 cards per box, Distributed by: APhrodisiac. UPC Code 644118128135. Recalled by SELECT DISTRIBUTIONS LLC. Units affected: 60 boxes.
Why was this product recalled?
Marketed without an approved NDA/ANDA: FDA analysis has found the product to be tainted with sildenafil
Which agency issued this recall?
This recall was issued by the FDA Drug on June 19, 2019. Severity: Critical. Recall number: D-1344-2019.