FDA recall D-1344-2019

Product

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

Distribution

MI, OH

Key facts

Status

Terminated

Initiation date

2019-04-09

Report date

2019-06-19

Termination date

2023-10-16

Voluntary/Mandated

Voluntary: Firm initiated

Location

Ferndale, MI, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1344-2019