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.
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.
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.
The capsules contain sildenafil, an ingredient approved for male sexual enhancement, but the product was not approved by the FDA. This unapproved use could lead to health risks such as adverse reactions or interactions with other medications.
People who purchased the THE ROCK capsules from Noah's Wholesale LLC or their distributor. Those with pre-existing conditions or who take medications that interact with sildenafil may be at higher risk.
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.
Look for the product name 'THE ROCK', 1200 mg strength, and the UPC code 6 61799 95052 7 on the blister card.
The FDA found the product to be unapproved due to containing sildenafil, which could pose health risks. It is not safe to use without FDA approval.
The recall record does not specify a remedy, so check the product details and contact the manufacturer if you have concerns.
Check for the product name 'THE ROCK', 1200 mg strength, and the UPC code 6 61799 95052 7 on the blister card.
We’ve drafted a message you can send Noah's Wholesale LLC to request your refund or repair — edit it as you like.
Subject: Recall D-0158-2024 — Noah's Wholesale LLC Noah's Wholesale LLC Hello, I own a Noah's Wholesale LLC that is covered by recall D-0158-2024 from Noah's Wholesale LLC. 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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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.
