FDAClass IJune 19, 2019

Aphrodisiac Platinum 40000 recall

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

Why was Aphrodisiac Platinum 40000 recalled?

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

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

All lots

Product
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
Quantity
60 boxes
Distribution
MI, OH
Recall date
June 19, 2019
Classification
Class I
Status
Terminated
Agency
FDA (drug)
Open FDA enforcement record Latest recalls