Reported Jun 6, 2018 · Terminated
POSEIDON Xtreme PLATINUM 4500,1000mg, packaged in single packs sold in 24-count boxes, Distributed by: Poseidon…
Shoreside Enterprises Inc.
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Shoreside Enterprises Inc. · 6345 Newtown Cir Apt A3 Ste A-3 · Tampa, FL · 33615-3629
Is this the product you have?
- POSEIDON Xtreme PLATINUM 4500,1000mg, packaged in single packs sold in 24-count boxes
- Distributed byPoseidon Distribution Atlanta, GA, UPC 638632428857
- Lot codes and dates
Lot #: 201117BLExp. 01/2020
- Amount recalled
- Unknown
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
Why it was recalled
Stop using this product now
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.
Using this product could cause serious injury, illness or death — stop using it now.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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