Better Weather Actives LLC has voluntarily recalled every lot of Better Weather Fix Elixir because the dietary supplement may contain undeclared kratom-related compounds capable of causing addiction, breathing suppression and other serious reactions. The company announced the nationwide recall on May 28, 2026, and the U.S. Food and Drug Administration published the notice the same day.
The action covers products sold in 15 ml bottles and packaged in display boxes labeled “Better Weather Fix Elixir” and “Better Weather Fix Elixir Berry.” They were distributed to consumers across the United States. Because all lots are included, buyers do not need to find a specific batch code before taking action.
Why Better Weather Fix Elixir was recalled
The products may contain mitragynine and mitragynine pseudoindoxyl, commonly shortened to MP, even though these substances were not declared on the label. Mitragynine is associated with kratom, while the recall notice describes MP as a more potent derivative of mitragynine.
The missing disclosure creates an additional safety concern because consumers may not know they have taken an active compound. They could combine the elixir with alcohol, prescription medicine, illicit drugs or another supplement without being able to assess the possible interaction.
Potential effects listed in the notice include nausea, vomiting, rapid heart rate, palpitations, anxiety, hallucinations, sedation and loss of consciousness. MP can suppress breathing and may cause a fatal reaction in severe cases.
The announcement further warns that mitragynine, particularly MP, may lead to addiction and severe opioid withdrawal symptoms. Taking these compounds alongside other drugs could increase the risk of serious or fatal physiological effects.
Recall timeline and affected products
The May 28 recall by Wyoming-based Better Weather Actives LLC applies to all lots of products sold in 15 ml bottles under the names “Better Weather Fix Elixir” and “Better Weather Fix Elixir Berry.” No expiration date or production batch has been excluded.
An earlier related recall was announced by Houston-based distributor XD Investments LLC on May 9 and published by the FDA on May 11. FDA analysis found undeclared mitragynine and MP in the products covered by that action.
The earlier recall involved approximately 448 boxes, including all flavors and variations sold through xdeor.com and maxensupplements.com between about November 9, 2025, and March 28, 2026. XD Investments said it stopped sales and distribution on April 1 and removed its remaining inventory from sale.
What consumers should do
Anyone who still has Better Weather Fix Elixir should stop using it immediately and return it to the place of purchase. A bottle should not be considered safe because it came from a different seller or carries a particular batch number.
Consumers with questions can contact Better Weather Actives at 208-495-4342 or recall@BetterWeatherActives.com between 9 a.m. and 5 p.m. Mountain Time, Monday through Friday.
People who experience breathing difficulty, a racing heartbeat, hallucinations, severe drowsiness, confusion, fainting or another concerning reaction should contact a healthcare provider. They should provide the complete product name and explain whether it was taken with medication, alcohol or another substance.
As of the May 28 announcement, Better Weather Actives had received no reports of adverse events associated with the recall. The absence of reported cases does not change the instruction to stop using the product.
Product descriptions, reported health risks and company contact details are available in the official FDA Better Weather Fix Elixir recall notice.
Why the scope of a recall matters
Some safety actions apply only to one production run. The MG217 eczema cream recall involving staph bacteria, for example, identified one affected lot. The Fix Elixir action is broader because every lot of the named supplement is included.
Other nationwide recalls cover an entire product range when the risk cannot be limited to selected batches. The Nara Organics infant formula recall similarly instructed consumers to stop using all lots and can sizes of the affected formula.
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What supplement buyers can learn
The Fix Elixir recall shows why consumers should keep original packaging and check federal notices when an ingredient concern emerges. Labels are essential for identifying active substances, reviewing possible interactions and helping healthcare professionals understand what a patient has taken.
A small bottle or wellness-focused claim does not establish that a supplement is free from potent ingredients. When a recall includes every lot, the safest response is to stop using the product rather than waiting for symptoms or additional warnings.
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