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Ram It and To The Moon Recall: What FDA Posted
Integrity Products of St. Louis, Missouri announced a recall on February 1, 2024 of capsules sold as male enhancement supplements. FDA analysis found sildenafil and tadalafil. FDA posted the notice on June 11, 2024. The risk is highest for men with diabetes, high blood pressure, high cholesterol or heart disease who take related medicines.
Written by the Stallion Power label deskUpdated · 4 min read
The recall facts
Capsules sold online as supplements held two prescription drugs, per FDA analysis.
We read the FDA recall posting. It carries a company announcement from February 1, 2024 and was posted by FDA on June 11, 2024. The posting is titled for male enhancement supplements. The products named are Ram It and To The Moon. We do not match a lot number to either name, because we did not read that detail.
| Item | Detail |
|---|---|
| Company | Integrity Products, St. Louis, Missouri |
| Company announcement | February 1, 2024 |
| FDA posting | June 11, 2024 |
| Finding | Sildenafil and tadalafil, per FDA analysis |
| Lot | HGW221116 |
| Format | Capsules in 10-count blister card boxes |
| Sold | Online, nationwide, as dietary supplements for male sexual enhancement |
| Adverse events | None reported by the company at announcement |
Who is at risk
The posting says men with diabetes, high blood pressure, high cholesterol or heart disease who take related medicines are at risk. This lines up with FDA's wording in other notices: sildenafil and tadalafil may interact with nitrates such as nitroglycerin and lower blood pressure to dangerous levels, and many people with those conditions take nitrates (FDA, X10 hidden-drug notice).
MedlinePlus says sildenafil must not be taken with nitrates used for chest pain (MedlinePlus, Sildenafil). If you took a recalled product and feel chest pain, faint, or have an erection lasting more than four hours, seek emergency care.
The gap between a label and the contents is the lesson. FDA does not approve dietary supplements before they are sold (FDA, Q&A on dietary supplements), and the NCCIH warns that sexual enhancement products may hold prescription drugs not on the label (NCCIH, Using Dietary Supplements Wisely).
What the recall does and does not tell us
| We know | We do not know |
|---|---|
| The drugs found, per FDA analysis | The amounts of each drug |
| One lot number was named | Whether other lots were affected |
| The format and box size | Whether the products are still sold |
| No adverse events were reported at announcement | What happened afterward |
A recall is a company action tied to FDA findings. It is not a court finding. We have not checked for any later legal case, and we say nothing about the company beyond the posting.
Stallion Power: from $49 a bottle30 gummies a bottle · 2, 3 or 6 bottles · free shipping on 3 or 6 · 60-day guarantee
See packsWhat to do if you have a similar product
- Check the box for the name and lot. Compare it with the posting.
- Stop use if it matches. Follow the recall instructions in the posting.
- Tell your doctor or pharmacist. List every medicine and supplement. See supplements and medications.
- Report reactions to MedWatch.
Stallion Power is a gummy with a printed Supplement Facts panel. We found no source showing hidden drugs in it, and we hold no lab report showing there are none. More cases are on tainted enhancement products.
Next step. Keep taking prescribed medicine, and ask a doctor before you add any enhancement product, especially if you take nitrates.
Who wrote this01
Written and reviewed by
Pages built from the label, the sales page and linked NIH, FDA, FTC, NIDDK, AHA and peer-reviewed sources.
Last updated . See our editorial standards and how we check reviews. This website is run by Gostallionpower, a Stallion Power U.S. merchant desk, not by the manufacturer or the distributor named on the label. We earn money when you buy through our order links.
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