Integrity Products recalls RAM IT dietary supplements containing undeclared sildenafil due to marketing without FDA approval. Consumers should check product labels for lot number HGW221116.
Marketed Without an Approved NDA/ANDA: Products contain undeclared sildenafil.
Integrity Products is recalling RAM IT dietary supplements that contain undeclared sildenafil. This poses a risk because these products were marketed without FDA approval, which could lead to serious health issues if taken without proper medical supervision.
These supplements contain undeclared sildenafil, a medication used to treat erectile dysfunction. Sildenafil can cause serious health issues like heart attacks or strokes, especially when combined with other medications or in people with heart conditions.
Anyone who owns or uses RAM IT dietary supplements with lot number HGW221116. People with heart conditions or who take medications that interact with sildenafil are at higher risk.
Check for the product name 'RAM IT', 1000 mg capsules, and the lot number HGW221116 on the box. The product was distributed by Integrity Products and sold between 2022 and 2025.
Look for the lot number HGW221116 on the box to confirm if your product is affected.
Reach out to Integrity Products at 1710 Fenpark Dr., Fenton, MO 63026 for further assistance.
The recall states that these supplements contain undeclared sildenafil, which can cause serious health issues. They are not safe to use without medical supervision.
Check the product label for lot number HGW221116. If it matches, contact Integrity Products for guidance.
Look for the product name 'RAM IT', 1000 mg capsules, and the lot number HGW221116 on the box.
We’ve drafted a message you can send Integrity Products to request your refund or repair — edit it as you like.
Subject: Recall D-0585-2024 — Integrity Products Integrity Products Hello, I own a Integrity Products that is covered by recall D-0585-2024 from Integrity Products. 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.
