PlainRecalls
FDA Drug Critical Class I Terminated

POSEIDON Xtreme PLATINUM 4500,1000mg, packaged in single packs sold in 24-count boxes, Distributed by: Poseidon Distribution Atlanta, GA, UPC 638632428857

Reported: June 6, 2018 Initiated: May 17, 2018 #D-0879-2018

Product Description

POSEIDON Xtreme PLATINUM 4500,1000mg, packaged in single packs sold in 24-count boxes, Distributed by: Poseidon Distribution Atlanta, GA, UPC 638632428857

Reason for Recall

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.

Details

Units Affected
Unknown
Distribution
Nationwide.
Location
Tampa, FL

Frequently Asked Questions

What product was recalled?
POSEIDON Xtreme PLATINUM 4500,1000mg, packaged in single packs sold in 24-count boxes, Distributed by: Poseidon Distribution Atlanta, GA, UPC 638632428857. Recalled by Shoreside Enterprises Inc.. Units affected: Unknown.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Drug on June 6, 2018. Severity: Critical. Recall number: D-0879-2018.