FDA Recall of Boner Bears Honey Male Enhancement Announced
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
The FDA has initiated a voluntary recall of Boner Bears Honey Male Enhancement due to undeclared sildenafil and Tadalafil, affecting products distributed in New Jersey.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on April 22, 2026 and geographically references New Jersey. Its severity classification of "high" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, cpsc, Food.
Recall Article
What Happened
The FDA announced a recall because analysis revealed the presence of undeclared sildenafil and Tadalafil in the product.
Which Products Are Affected
The affected product is Boner Bears Honey Male Enhancement 100% Wildflower Honey, sold in boxes containing 15 pouches, each with Net Wt 15 G. It has UPC 788362191603, Lot # BBH0128, and expiration date 01/28. The product was manufactured in Florida and distributed in New Jersey, with an unknown quantity affected. The official recall number is H-0653-2026.
What You Should Do
Consumers should immediately stop using the product and contact the recalling firm, Pure Vitamins and Natural Supplements, LLC, at their address: 1708 E North Bay St, Tampa, FL 33610-7539, for information on returns or refunds, as the firm initiated the recall via methods including email, fax, letter, press release, telephone, or visit.
Why This Matters
This recall is classified as Class I by the FDA, indicating a situation where there is a reasonable probability of serious adverse health consequences due to the undeclared ingredients.
Source
FDA Recall Notice H-0653-2026
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,155 characters here).
Similar severity timing
Same severity (high) notices issued closest in time to April 22, 2026.
Frequently Asked Questions
Common questions about this FDA recall.