Shoreside Enterprises Inc. recalls 7K capsules packaged in single packs sold in 24-count boxes, Distributed by SX Power Co. San Diego, CA 92108, UPC
FDA recalls 7,000 Shoreside Enterprises 7K capsules (24-count boxes) due to unapproved sildenafil and tadalafil. Products marketed without FDA approval pose safety risks.
Recall notice
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.
Contact the company & request your remedy
What happened, in plain English
Shoreside Enterprises is recalling 7,000 capsules sold in 24-count boxes because they contain undeclared sildenafil and tadalafil without FDA approval. These products lack safety and efficacy testing, making them potentially risky for users. Read more at govinfonow.com/recall/40520-shoreside-enterprises-7k-capsules-recall-unapproved-sildenafil-and-tadalafil-found.
Source Summary by GovInfoNow · govinfonow.com/recall/40520-shoreside-enterprises-7k-capsules-recall-unapproved-sildenafil-and-tadalafil-found · Updated October 7, 2026 · FDA enforcement record: FDA #D-0880-2018
Cite this page
“Shoreside Enterprises 7K Capsules Recall: Unapproved Sildenafil and Tadalafil Found.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/40520-shoreside-enterprises-7k-capsules-recall-unapproved-sildenafil-and-tadalafil-found. Based on FDA recall #D-0880-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0880-2018%22&limit=1).
Why it’s dangerous
The capsules contain sildenafil (Viagra) and tadalafil (Cialis) without FDA approval. These drugs have not been tested for safety and effectiveness, so they could cause health issues like heart problems or interactions with other medications.
Who’s affected
People who purchased these capsules from retailers in the U.S. are affected. Those with medical conditions or using other medications may be at higher risk due to untested drug combinations.
How to tell if you have this one
Check for 7K capsules in single packs sold in 24-count boxes with UPC 601577513148. Products distributed by SX Power Co. in San Diego, CA, with lot number RO and expiration 12/31/2021 are recalled.
- Brand
Shoreside Enterprises- Product
7K capsules packaged in single packs sold in 24-count boxes, Distributed by SX Power Co. San Diego, CA 92108, UPC- Category
Drug
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class I- Status
Terminated- Distribution
Nationwide.
| Recall number | Product, codes & lots |
|---|---|
| D-0879-2018 | POSEIDON Xtreme PLATINUM 4500,1000mg, packaged in single packs sold in 24-count boxes, Distributed by: Poseidon Distribution Atlanta, GA, UPC 638632428857; Lot #: 201117BL, Exp. 01/2020 |
| D-0880-2018 | 7K capsules packaged in single packs sold in 24-count boxes, Distributed by SX Power Co. San Diego, CA 92108, UPC 601577513148; Lot #: RO, Exp. 12/31/2021 |
What to do — step by step
Check Product Details
Look for the UPC 601577513148 on the box and lot number RO with expiration 12/31/2021.
Questions people ask
Why is this product being recalled?
FDA analysis found the capsules contain undeclared sildenafil and tadalafil without FDA approval, so they lack safety and efficacy testing.
Are these capsules safe to use?
No, these capsules are unapproved drugs that have not been tested for safety and effectiveness, so they could cause health risks.
How can I tell if I have the recalled product?
Check for 7K capsules in single packs sold in 24-count boxes with UPC 601577513148, lot number RO, and expiration 12/31/2021.
Contact Shoreside Enterprises
We’ve drafted a message you can send Shoreside Enterprises to request your refund or repair — edit it as you like.
Subject: Recall D-0880-2018 — Shoreside Enterprises 7K capsules packaged in single packs sold in 24-count boxes, Distributed by S Hello, I own a 7K capsules packaged in single packs sold in 24-count boxes, Distributed by SX Power Co. San Diego, CA 92108, UPC that is covered by recall D-0880-2018 from Shoreside Enterprises. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0880-2018 (May 17, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0880-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.