Eros Apothecary of Indio, California, is recalling its Candy Power For Man Organic Honey dietary supplement because the product contains tadalafil that is not listed on the label, according to a notice posted Nov. 12, 2026, by the U.S. Food and Drug Administration.
Tadalafil is the active ingredient in the prescription drug Cialis, which is used to treat erectile dysfunction. The notice says the drug is approved only for use under the supervision of a licensed health care professional. It says the undeclared tadalafil may interact with nitrates, which are in certain prescription medicines including nitroglycerin, and cause a dangerous drop in blood pressure. According to the notice, medicines that contain nitrates are often taken by people who have heart disease, diabetes, high cholesterol or high blood pressure.
Recalled product details
Detail
Information
Product
Candy Power For Man Organic Honey
Packaging
Yellow and orange, 60 individually wrapped candies
Batch
241020
Manufacturing date
January 2024
Expiration date
December 2029
UPC
5285002251390
Where sold
eBay
Dates sold
April 27, 2026, to July 20, 2026
Source: U.S. Food and Drug Administration.
The recall began after FDA laboratory testing found the undeclared tadalafil. The notice does not say how many units are affected or whether anyone has reported illness.
According to the company announcement, the product was sold on eBay between April 27, 2026, and July 20, 2026. It comes in yellow and orange packaging that holds 60 individually wrapped candies. The back panel lists batch 241020, a manufacturing date of January 2024, an expiration date of December 2029 and UPC 5285002251390.
The notice tells consumers to stop using Candy Power For Man immediately and dispose of any remaining product. People with questions can email Eros Apothecary at ErosFDA@gmail.com. People who have had health problems that may be related to the product should contact their health care provider.
Adverse reactions or quality problems can be reported to the FDA’s MedWatch Adverse Event Reporting program. Reports can be filed online at www.fda.gov/medwatch/report.htm, or by mail or fax using a form available from the FDA. The form can be requested by calling 1-800-332-1088. The notice says the recall is being conducted with the knowledge of the FDA.
