Shoreside 7K Capsules Recalled for Undeclared Drugs
FDA recalls Shoreside Enterprises 7K capsules due to undeclared sildenafil and tadalafil. Check your UPC and lot number for details.
Stop using this 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.
Contact the company
What happened, in plain English
Shoreside Enterprises Inc. is recalling 7K capsules because they contain undeclared sildenafil and tadalafil, which are active ingredients in prescription drugs. The FDA found these products were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA). Because the safety and efficacy of these unapproved drugs have not been established, the products are subject to recall. Read more at govinfonow.com/recall/40520-shoreside-7k-capsules-recalled-for-undeclared-drugs.
Source Summary by GovInfoNow · govinfonow.com/recall/40520-shoreside-7k-capsules-recalled-for-undeclared-drugs · Updated October 11, 2026 · FDA enforcement record: FDA #D-0880-2018
Cite this page
“Shoreside 7K Capsules Recalled for Undeclared Drugs.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/40520-shoreside-7k-capsules-recalled-for-undeclared-drugs. 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 undeclared sildenafil and tadalafil, which can cause serious health issues if taken with other medications or by people with certain heart conditions. Since the products were not approved by the FDA, their safety and efficacy have not been established.
Who’s affected
Consumers who purchased 7K capsules packaged in single packs sold in 24-count boxes distributed by SX Power Co. in San Diego, CA. Individuals taking these capsules for sexual health purposes are at risk of unintended drug interactions.
How to tell if you have this one
Look for 7K capsules packaged in single packs sold in 24-count boxes. The product was distributed by SX Power Co. in San Diego, CA 92108. Check for UPC 601577513148 and Lot # RO with an expiration date of 12/31/2021.
- 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
Stop Using the Product
Discontinue use of the recalled 7K capsules immediately due to the presence of undeclared active ingredients.
Check Your Product Details
Verify if you have the affected product by checking for UPC 601577513148, Lot # RO, and an expiration date of 12/31/2021.
Consult a Healthcare Provider
If you have taken these capsules, speak with your healthcare provider about potential health risks associated with undeclared sildenafil and tadalafil.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 2.1 years after the firm started it.
- Firm started the recall
- Published in FDA’s Enforcement Report
- FDA classified it Class I
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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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 qwen3.6:35b-a3b on October 11, 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.