Shoreside Enterprises Inc. recalls POSEIDON Xtreme PLATINUM 4500,1000mg, packaged in single packs sold in 24-count boxes, Distributed by: Poseidon Distribu
Recalled June 6, 2018 · FDA recall D-0879-2018 · Shoreside Enterprises
Hazard
Marketed Without An Approved NDA/ANDA: FDA analysis found products to contain undeclared sildenafil and tadalafil. The presence of sildenafil and tadalafil makes these products an unapproved drug for which safety and efficacy have not been established and, therefore, subject to recall. · FDA Class I
Units
Unknown
Sold at
Nationwide.
Description
Marketed Without An Approved NDA/ANDA: FDA analysis found products to contain undeclared sildenafil and tadalafil. The presence of sildenafil and tadalafil makes these products an unapproved drug for which safety and efficacy have not been established and, therefore, subject to recall.
Product
POSEIDON Xtreme PLATINUM 4500,1000mg, packaged in single packs sold in 24-count boxes, Distributed by: Poseidon Distribution Atlanta, GA, UPC 638632428857
Manufacturer(s)
Shoreside Enterprises Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →