Recall - Candy Power For Man (Honey Dietary Supplement) produced by Eros Apothecary - Contain Undeclared Tadalafil

Summary

Company Announcement

Eros Apothecary of Indio, California is recalling Candy Power For Man Organic Honey because the product was found to contain undeclared tadalafil.

Tadalafil is the active ingredient in the FDA-approved prescription drug Cialis, used to treat erectile dysfunction. FDA approval of Cialis is restricted to use under the supervision of a licensed health care professional. The undeclared tadalafil may interact with nitrates found in certain prescription medications, such as nitroglycerin, and cause a dangerous drop in blood pressure. People with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrate-containing medications.

The product was sold via eBay between April 27, 2026, and July 20, 2026.

The Candy Power For Man Organic Honey is packaged in yellow and orange packaging, containing 60 individually wrapped candies. The following identifying information appears on the back panel of the product packaging:

• Batch: 241020
• Manufacturing Date: January 2024
• Expiration Date: December 2029
• UPC: 5285002251390

The recall was initiated after FDA laboratory testing identified undeclared tadalafil. Consumers should stop using Candy Power For Man immediately and dispose of any remaining product.

Consumers with questions regarding this recall may contact Eros Apothecary at [email protected] Consumers who have experienced health problems potentially related to this product should contact their healthcare provider.

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: www.fda.gov/medwatch/report.htm

Regular Mail or Fax: Download form www.fda.gov/MedWatch/getforms.htm 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.