Unrated Drug recall · FDA · Published October 16, 2023

Noah's Wholesale THE ROCK Capsules: Unapproved Sildenafil Risk

FDA recalls Noah's Wholesale LLC's THE ROCK Male Sexual Performance Capsules (1200mg) due to unapproved sildenafil content. These capsules are not FDA-approved and may pose health risks.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #D-0158-2024Drug Noah's Wholesale LLC ›

Recall notice

Marketed Without an Approved NDA/ANDA: FDA analysis found the product to be tainted with Sildenafil an ingredient found in an FDA approved product for the treatment of male sexual enhancement, making this an unapproved drug.

Take action

Contact the company

Recalling firmNoah's Wholesale LLC4720 Nw 165th St · Miami Lakes, FL 33014-6423

✎ GovInfoNow plain-language explainer

Noah's Wholesale LLC recalled their THE ROCK Male Sexual Performance Enhancement Capsules (1200mg) because they contain sildenafil without FDA approval. This makes them an unapproved drug that could pose health risks. Read more at govinfonow.com/recall/33061-noah-s-wholesale-the-rock-capsules-unapproved-sildenafil-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/33061-noah-s-wholesale-the-rock-capsules-unapproved-sildenafil-risk · Updated August 17, 2026 · FDA enforcement record: FDA #D-0158-2024

Cite this page

“Noah's Wholesale THE ROCK Capsules: Unapproved Sildenafil Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/33061-noah-s-wholesale-the-rock-capsules-unapproved-sildenafil-risk. Based on FDA recall #D-0158-2024 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0158-2024%22&limit=1).

The Food and Drug Administration announced on Oct. 16, 2023, that Noah's Wholesale LLC is recalling THE ROCK, Male Sexual Performance Enhancement Capsules because they are tainted with Sildenafil, an unapproved ingredient. The FDA said the product is marketed without an approved New Drug Application or Abbreviated New Drug Application.

How to tell if you have it

THE ROCK, Male Sexual Performance Enhancement Capsules, 1200 mg, 1 count blister card, Distributed by Steele
UPC 6 61799 95052 7
Lot# 03032021
Expiration date: 12/31/2027

The hazard

The FDA said the product is tainted with Sildenafil, an ingredient found in an FDA-approved product for the treatment of male sexual enhancement. This makes the capsule an unapproved drug.

Context

GovInfoNow's records show other recent recalls of similar products include StuffbyNainax MR 7 SUPER 700000 Capsules (2025-12-15) and SILINTAN 25-pill bottle (2025-10-20). Additional recent actions involve Buy-Herbal Kian Pee Wan Capsules Recall (2026-03-21).

How to tell if you have this one

Check for the product name 'THE ROCK', 1200 mg strength, and the UPC code 6 61799 95052 7. The capsules were distributed by Steele Productions from Hallandale, FL with a lot number of 03032021 and expire December 31, 2027.

Brand
Noah's Wholesale LLC
Product
THE ROCK, Male Sexual Performance Enhancement Capsules, 1200 mg, 1 count blister card, Distributed by Steele
Category
Drug

Based on the official FDA remedy

What to do — step by step

Check Product Details
Look for the product name 'THE ROCK', 1200 mg strength, and the UPC code 6 61799 95052 7 on the blister card.

Where it went and when

Where it was distributed

Distributed in Florida, and outside the U.S.

FDA distribution: “Florida, Bahamas, Turks & Caicos Islands” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Florida.

Recall timeline

FDA published this recall 2 months after the firm started it.

Oct 16, 2023Firm started the recall
Dec 21, 2023FDA classified it Class I
Dec 27, 2023Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Link to this recall

<a href="https://govinfonow.com/recall/33061-noah-s-wholesale-the-rock-capsules-unapproved-sildenafil-risk">Noah's Wholesale THE ROCK Capsules: Unapproved Sildenafil Risk (GovInfoNow)</a>

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-0158-2024 (October 16, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0158-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 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.