Boner Bears Lawsuit and Male Enhancement Supplement False Advertising Claims

Male enhancement products are sold online, in convenience stores, and at gas stations as gummies, honey packets, chocolates, coffee, and pills. Many are labeled as a dietary supplement or "natural herbal" blend. The problem regulators keep finding is that some of them work because they secretly contain prescription erectile dysfunction drugs.

According to the FDA, many products that claim to help with sexual enhancement, such as male enhancement supplements, male energy pills, and stamina pills, are likely to be contaminated with dangerous hidden ingredients. The most common are sildenafil (the drug in Viagra) and tadalafil (the drug in Cialis), sometimes at doses above what a doctor would prescribe.

That creates two kinds of legal claims:

• False advertising and mislabeling. People paid for a natural supplement and got an unlabeled prescription drug. This is a consumer fraud theory, often brought as a class action.
• Personal injury. Someone who takes nitrate heart medicine, or has a condition that rules out these drugs, can be seriously harmed by a dose they did not know they were taking.

These products are also a health risk, not just a money issue. The FDA warns that sildenafil and tadalafil can interact with nitrates found in some prescription drugs, such as nitroglycerin, and lower blood pressure to dangerous levels, and that people with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates.

Boner Bears is a brand name used on several product types. The FDA's records in 2026 tie it to more than one seller:

Boner Bear Honey

On March 14, 2026, Pure Vitamins and Natural Supplements, LLC of Tampa, Florida voluntarily recalled Boner Bear Honey, along with Red Bull Extreme and Blue Bull Extreme honey products. The company said FDA laboratory analysis confirmed that Boner Bear Honey contained sildenafil and tadalafil, and the other two contained sildenafil, none of it listed on the label. These were sold as single-serving tubes of sexual enhancement honey. The FDA also posted a public notification on March 30, 2026, that Boner Bears Honey may be harmful due to hidden drug ingredients.

Boner Bears Chocolate

The FDA posted a notification on February 13, 2026, that Boner Bears Chocolate may be harmful due to a hidden drug ingredient. On May 21, 2026, JXK Enterprises, Inc. recalled Boner Bears Sex Chocolate, Lot BB21125, expiration 02/2026, after FDA testing confirmed undeclared sildenafil; it had been sold nationwide online.

Boner Bears gummies

The original Boner Bears product was a gummy marketed as an herbal remedy. That product was the subject of the 2023 class action described below, which alleged it contained tadalafil.

Other male enhancement products

Boner Bears is one name on a long list. The FDA's sexual enhancement notification list shows warnings in 2026 alone for products including Hard AF!, Big Dick Energy!, X10 Natural Enhancement Supplement, Erectus Plus, Sensual Miracle Honey, MAGNUM brand products, Premium OrgaZEN 10000, Anaconda Premium 500K, MAXMAN Coffee, and several chocolates marketed to men. Earlier notices covered Rhino-branded gummies and pills and many "miracle honey" products. A recall or notice is not a court finding, but it is strong evidence of what was in the product.

The case was Keegan v. Minahan, No. 23-60501-Civ-Scola, in the U.S. District Court for the Southern District of Florida. The plaintiff, a New Jersey man, said he bought Boner Bears in July 2022 relying on claims that it contained only natural ingredients, and then had a headache, dizziness, and blurred vision. He said he has medical conditions that prevent him from taking tadalafil.

The complaint sued Daniel P. Minahan, whom it described as the leader of the business; Perk Industries Inc., which it said held the Boner Bears trademark; and Innovative Health Labs Inc., which it said made and shipped the product from Fort Lauderdale. It alleged that Boner Bears was sold as "a proprietary blend of organic ingredients" while actually containing a substantial dose of tadalafil, and sought to represent everyone in the United States who bought Boner Bears in the prior six years.

On June 7, 2023, Judge Robert N. Scola Jr. dismissed the complaint without prejudice because its single common law fraud claim was not pleaded with the detail that Federal Rule of Civil Procedure 9(b) requires, and he did not grant leave to amend because none was requested. The court did not decide whether Boner Bears contained tadalafil. A dismissal without prejudice means the claim was not decided on the merits, but this case did not produce a settlement or payment.

We could not find another Boner Bears class action pending as of September 2026. The 2026 FDA recalls, which involve different sellers, could support new claims.

The strongest cases usually have three parts:

1. A tainted product you can prove you took. The best evidence is a product and lot named in an FDA recall or public notification, plus your package or receipt.
2. A real injury. Examples include fainting or a dangerous blood pressure drop, heart problems, a prolonged painful erection needing emergency care, or vision or hearing changes. Injuries are more serious for people taking nitrates or alpha blockers.
3. A defendant who can be found and can pay. Many of these brands are small online sellers or importers. Retailers and distributors may also be responsible under state law.

If you were not hurt, you may still have a claim for what you paid, because you bought a "natural" product and got an undisclosed drug. Individually, those amounts are small, which is why they are usually brought as class actions. As the Keegan case shows, those suits need specific facts about the ads, the purchase, and the testing to survive.

You probably do not have a claim if your product was never tested or named by the FDA, if you knew it contained a drug, or if you had no injury and no receipt. See how to tell whether you qualify.

Who may be responsible

These products pass through several hands, and claims can reach more than the brand owner. The Keegan complaint, for example, named the individual it said led the business, the company it said held the trademark, and the company it said manufactured and shipped the product. The 2026 recalls came from yet other sellers: a Tampa honey distributor and an online chocolate seller. Depending on state law, the importer, distributor, and the website or store that sold the product may share responsibility. Knowing exactly where you bought the product, and keeping the order confirmation, helps an attorney figure out who can be sued. It also matters because many small sellers disappear or lack insurance, which can make it hard to collect even a strong claim.

There is no Boner Bears settlement and no claim form. Any money would come from a new lawsuit.

• Personal injury: medical bills, lost wages, and pain and suffering, depending on the harm.
• Consumer class claims: refunds of the purchase price, sometimes with statutory damages under state consumer laws. Individual amounts tend to be small.
• Government refunds: the FTC sometimes returns money to buyers of deceptively marketed supplements.

A real example of the last category: in August 2012, the FTC mailed 153,109 checks, totaling over $6 million, to people who bought deceptively advertised supplements, including Spontane-ES, which was marketed as clinically proven to treat 90 percent of men with erectile dysfunction. Refunds like that follow years of enforcement and are not common. See whether class actions are worth it for how small consumer recoveries usually work.

Several layers of law apply:

• Federal drug law. A product that contains sildenafil or tadalafil is not a legal dietary supplement. The FDA treats these as products with hidden drug ingredients and notes that Viagra and Cialis are approved only for use under a licensed health care professional's supervision. The FDA enforces this; consumers generally cannot sue under the federal drug law directly.
• The FTC Act. Section 5 bans deceptive advertising, and the FTC requires health claims to be backed by evidence.
• State consumer protection laws. These let buyers sue for deceptive labels such as "all natural" on a product with a hidden drug, and some provide minimum damages or attorney fees.
• Fraud and product liability. Common law fraud, failure to warn, and defective product claims support injury cases. As Keegan shows, a fraud claim must describe the false statements, when and where they were made, and how the buyer relied on them.

For the difference between a regulator's recall and a private lawsuit, see recall vs. class action.

Each state sets its own deadline, and the clock usually starts when you were hurt or learned the product caused it. In California, for example, a personal injury claim generally must be filed within two years under Code of Civil Procedure section 335.1. Consumer fraud deadlines differ and are sometimes longer.

1. Stop using the product and talk to a doctor if you had symptoms, especially if you take heart or blood pressure medicine.
2. Keep the package, lot number, and any leftover product in a sealed bag. It may be tested.
3. Save proof of purchase and screenshots of the product listing.
4. Report it. You can report side effects to the FDA's MedWatch program, which also creates a record. You can also report deceptive marketing to the FTC.
5. Check the FDA list. Search the FDA's sexual enhancement product notifications for your product name before assuming it is safe or tainted.
6. Be wary of settlement pitches. There is no Boner Bears settlement; see how to spot settlement scams.

A free case review takes about two minutes. You can also read about supplement mislabeling lawsuits or browse other lawsuits you may be able to join.