Food recall

JXK Enterprises, Inc. recall: Boner Bears CHOCOLATE

JXK Enterprises, Inc., of Miami, FL, recalled Boner Bears CHOCOLATE. The FDA's reason: “JXK Enterprises, Inc is voluntarily recalling Boner Bears Chocolate, Lot #BB21125, after being notified that FDA laboratory analysis confirmed the presence of sildenafil, an active ingredient in...” The FDA classified it Class I: it could cause serious harm or death. The company began the recall voluntarily on May 21, 2026, and the FDA first listed it in its Enforcement Report of November 4, 2026. The recall is still going on.

How serious

Class I

It could cause serious harm or death

Why

Other ingredient not on the label (sulfites, dyes...)

Status

Ongoing

The recall

Company
JXK Enterprises, Inc. (Miami, FL)
Reason, in FDA's words
“JXK Enterprises, Inc is voluntarily recalling Boner Bears Chocolate, Lot #BB21125, after being notified that FDA laboratory analysis confirmed the presence of sildenafil, an active ingredient in the FDA-approved prescription drug Viagra, which is not declared on the product label.”
Where it was sold
Boner Bears Chocolate is marketed as a sexual enhancement product and was distributed nationwide via online sales through www.elyxr.com.
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
99495

The product recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • H-0186-2027 Class I

    Boner Bears CHOCOLATE, 3 DOSES PER BAR, NET WT. 22g, MALE ENHANCEMENT, DOSAGE: Consume 1 piece at least 1 hour prior to activity. Do not exceed 1 piece in any 48 hour period. Serving size about 7 g

    Codes: Lot #BB21125

    Quantity: Unknown

Get new charts weekly

One email a week with the newest charts and their key numbers. No account needed.

Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of November 4, 2026.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.