Boner Bears Honey Male Enhancement 100% Wildflower Honey

Pure Vitamins and Natural Supplements, LLC has recalled Boner Bears Honey Male Enhancement 100% Wildflower Honey, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on April 15, 2026 and was initiated on March 13, 2026. It is classified as a Class I recall, which means there is a reasonable chance that using this product could cause serious health problems or death.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers Boner Bears Honey Male Enhancement 100% Wildflower Honey, with approximately Unknown affected. The company behind the recall is Pure Vitamins and Natural Supplements, LLC, based in Tampa, FL. The FDA describes the product as: “Boner Bears Honey Male Enhancement 100% Wildflower Honey, total of 15 pouches per box, Net Wt 15 G each pouch. Dosage: Consume 1 entire pouch 30 minutes before Intercourse. MANUFACTURED IN: FLORIDA. UPC 788362191603”

Why was Boner Bears Honey Male Enhancement 100% Wildflower Honey recalled?

According to the FDA, the stated reason for the recall is: “FDA analysis revealed the presence of undeclared sildenafil and Tadalafil.” In plain terms, this recall relates to an undeclared ingredient or allergen.

An undeclared ingredient means a food contains something — often a major allergen such as milk, eggs, soy, wheat, peanuts, or tree nuts — that is not listed on the label. For most people this is not dangerous, but for someone with a food allergy or sensitivity it can trigger a serious reaction. Accurate labeling is required so that people can avoid ingredients they need to stay away from.

What should you do?

If you think you may have bought Boner Bears Honey Male Enhancement 100% Wildflower Honey, compare it against the product description and identifying codes (Lot # BBH0128 EXP 01/28) before using it. This recall is currently listed as ongoing.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Pure Vitamins and Natural Supplements, LLC or your local health authority.

About this recall

This recall was distributed in FL. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.