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RECALL: Ram It & To The Moon -Male Enhancement Supplements

6/11/24 Ram It & To The Moon male enhancement supplements recalled as they are tainted with sildenafil and Tadalafil, a FDA approved drug for the treatment of erectile dysfunction. As the FDA did not approve it's inclusion in Ram It & To the Moon for safety and efficacy, they are subject to recall.


Risk Statements: Men with diabetes, high blood pressure, high cholesterol, or heart disease, may be on medications that if taken with these products could lower blood pressure to dangerous levels that could be life threatening. The products affected are men with diabetes, high blood pressure, high cholesterol, or heart disease.


To date, Integrity Products. has not received any reports of adverse events related to this recall.


The product is marketed as dietary supplements for male sexual enhancement and is packaged in a blister card. 10 count boxes. Ram It & To The Moon were distributed to consumers nationwide via the Internet. We are notifying the public through this public announcement due to lack of ability to identify customers who may have received the product.


ACTION

Integrity Products. is notifying its customers that have the Ram It & To The Moon products to stop use and properly discard the product. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.


CONTACT

Consumers with questions regarding this recall can contact Integrity Products. at integrityproductsusa@gmail.com, St Louis MO Monday – Friday 9am to 9pm Eastern Standard Time


Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

  • Complete and submit the report Online

  • Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Link to FDA Advisory

Link to FDA Advisory

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