Honey recalled after FDA detects active ingredient to treat erectile dysfunction in product

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Shopaax.com in Newark, DE is recalling all lots of Kingdom Honey Royal Honey VIP because it contains undeclared sildenafil, the active ingredient in Viagra, an FDA-approved prescription drug used to treat erectile dysfunction.

The recall was initiated after an FDA lab analysis confirmed that Kingdom Honey Royal Honey VIP contains sildenafil.

The FDA issued a warning letter to the company, along with three other honey companies, about the presence of active drug ingredients in their products.

FDA approval of Viagra is limited to use under the supervision of a licensed healthcare professional. Use of products containing the undeclared active ingredient may pose a threat to consumers, as the active ingredient may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may cause a significant drop in blood pressure life-threatening blood pressure. People with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. Among the adult male population most likely to use these products, adult men who use nitrates for heart problems have the highest exposure to these products.

Recalled products:

  • The product comes in a golden box and contains 12 sachets of 20 grams of honey with different expiry dates stamped on the back.
  • It is promoted and sold for sexual enhancement on various websites including www.shopaax.com and possibly some retail stores.
  • The company started selling this product on Shopaax.com on 02/2021 and was suspended on 07/2022.

The sale of this product has been suspended.

The company has temporarily removed all other products from the website pending an investigation. Product may still be available on other websites and retail stores.

Consumers who purchased Kingdom Honey Royal Honey VIP from Shopaax.com are urged to immediately stop using and return the recalled products.

Consumers should contact their physician or health care provider if they have had any problems that may be related to taking or using this product.

Have you had a reaction to this product?

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 On line
  • Ordinary mail or fax: Download the form or call 1-800-332-1088 to request a report form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178

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