The Recall Desk
SevereFDA (Food)·H-0653-2026·Announced 2026-04-15

Boner Bears Honey Male Enhancement contains undeclared pharmaceutical drugs

Pure Vitamins and Natural Supplements, LLC is recalling Boner Bears Honey Male Enhancement because FDA testing found undeclared sildenafil and tadalafil, prescription drugs not listed on the label.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: FDA Class I recall with undeclared pharmaceutical drugs (sildenafil and tadalafil) that pose serious health risks including potential drug interactions, meeting the Severe criterion for Class I recalls with significant risk of harm.

Plain-English summary

Pure Vitamins and Natural Supplements, LLC is recalling Boner Bears Honey Male Enhancement 100% Wildflower Honey (UPC 788362191603, Lot # BBH0128, EXP 01/28). FDA analysis revealed the presence of undeclared sildenafil and tadalafil in the product.

Sildenafil and tadalafil are prescription pharmaceutical ingredients not declared on the product label. These ingredients can interact with other medications and pose health risks to consumers who do not know they are consuming them.

The product was distributed in New Jersey. Consumers who have purchased this product should stop using it immediately and consult their healthcare provider if they have concerns about their health or potential medication interactions.

The recalled product

Product
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
Manufacturer
Pure Vitamins and Natural Supplements, LLC
Category
Food — Supplement / Dietary Product
Hazard
  • undeclared-pharmaceutical
  • sildenafil
  • tadalafil
  • drug-interaction

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • Lot # BBH0128 EXP 01/28

Distribution

Distribution scope not specified by the agency.

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