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People across the country may have been exposed to a dangerous stimulant after buying Rapture Pre Workout supplements from Leader Formulas, LLC. The company recalled three flavors after the FDA found 1,3-dimethylamylamine (DMAA), which is not allowed in dietary supplements. DMAA can raise blood pressure and lead to serious heart problems, such as chest tightness, trouble breathing, and heart attacks. The recalled products were sold nationwide in stores and online from January 29, 2025, to May 25, 2026. If you had serious health problems after using these supplements, you may want to look into a product liability lawsuit.
This recall brings up questions about how these supplements are made, how ingredients are tested, and whether consumers are kept safe. People who bought Rapture Pre Workout may not have known they were taking something the FDA has warned about for over ten years.
Parker Waichman LLP is a national law firm that helps people hurt by unsafe or defective products. If you were injured after using these recalled supplements, you may be able to seek compensation, depending on your situation and medical proof.
The recall involves three flavors of Rapture Pre Workout, each sold in a 450-gram container bearing lot number 260327-4.
| Recalled product | UPC |
| Rainbow Twist | 710154236506 |
| Electric Lemonade | 710143236513 |
| Berry Mojito | 710154236544 |
Consumers should compare the product name, flavor, lot number, and UPC with the official recall information.
The FDA published the company’s recall announcement on October 7, 2026. The company reported that it had not received adverse-event reports associated with the recall as of the announcement. However, that statement does not establish whether every consumer who experienced symptoms reported them to the manufacturer.
Consumers should stop using recalled supplements immediately. Those who believe they suffered injuries should photograph the packaging, preserve purchase records, and consult an attorney about retaining the product as potential evidence before returning it for a refund.
DMAA, also called 1,3-dimethylamylamine or methylhexanamine, is a stimulant previously marketed in supplements intended to increase energy, support weight loss, and improve athletic performance.
DMAA can narrow blood vessels and increase blood pressure, placing additional strain on the cardiovascular system. These effects are particularly concerning when consumers take stimulant-containing supplements before strenuous exercise.
The FDA has warned about DMAA since at least 2013. The agency considers dietary supplements containing DMAA adulterated under federal law because DMAA is not a lawful dietary ingredient.
Under 21 U.S.C. § 342, dietary supplements containing certain unlawful or unsafe ingredients may be classified as adulterated. Manufacturers are responsible for ensuring their products comply with applicable federal safety requirements.
The FDA previously issued a warning on May 5, 2026, after identifying undeclared DMAA in Rapture Preworkout. This earlier warning may be relevant to investigations concerning manufacturer knowledge, ingredient disclosures, and regulatory compliance.
DMAA exposure can produce cardiovascular effects that may become dangerous, particularly for individuals with underlying medical conditions or those combining supplements with additional stimulants.
Potential medical complications associated with DMAA include:
These conditions are not confirmed injuries caused by the recalled Rapture products. Establishing a connection between a particular supplement and an individual’s medical condition requires appropriate medical evidence.
Consumers experiencing chest pain, severe breathing difficulties, fainting, or symptoms of a stroke should seek emergency medical attention immediately.
Pre-workout supplements are frequently consumed shortly before intense physical activity. Exercise naturally increases heart rate, blood circulation, and the body’s oxygen requirements.
Adding a powerful stimulant may increase cardiovascular stress, particularly when consumers also drink coffee, energy drinks, or other stimulant-containing products.
Dehydration, high temperatures, underlying heart conditions, and excessive stimulant consumption may further complicate the risks.
Consumers who experience dizziness, unusual heartbeats, chest discomfort, or shortness of breath during exercise may initially attribute these symptoms to physical exertion.
For this reason, medical professionals evaluating a cardiovascular emergency should be informed about any pre-workout supplements consumed before symptoms developed.
The FDA’s discovery of DMAA may provide important evidence, but a recall does not automatically establish civil liability. Injured consumers must generally demonstrate that the product caused their injuries and that the legal requirements for their claims are satisfied.
Depending on the evidence and applicable state law, potentially responsible parties may include the supplement manufacturer, ingredient suppliers, distributors, or retailers.
Attorneys investigating these cases may examine laboratory results, ingredient sourcing records, manufacturing procedures, quality control documents, and communications concerning product safety.
The FDA’s earlier warnings about DMAA may also become relevant when determining whether a company knew or reasonably should have known about the substance’s risks.
Identifying the appropriate defendants requires examining each company’s role in producing and distributing the affected supplements.
Consumers who establish that a defective supplement caused their injuries may be entitled to compensation for medical expenses, lost income, and other damages recognized under applicable state law.
Recoverable medical expenses may include emergency treatment, hospitalization, diagnostic testing, medication, rehabilitation, and reasonably necessary future medical care.
Individuals who cannot work because of their injuries may seek lost wages or compensation for diminished earning capacity.
Depending on state law, damages may also include physical pain, emotional suffering, permanent disability, and reduced quality of life.
If a supplement-related injury results in death, eligible surviving family members or estate representatives may have grounds to pursue a wrongful death or survival claim.
Compensation depends on the severity of the injuries, the available evidence, and the laws governing the claim.
Evidence is essential when determining whether a recalled supplement caused or contributed to an injury.
Attorneys may review medical records, emergency department reports, blood pressure measurements, cardiac testing, and physician assessments.
Purchase receipts, online order confirmations, photographs, product containers, and remaining supplements may help establish exposure to the recalled product.
Medical professionals may also evaluate whether the timing and nature of the injury are consistent with DMAA exposure while considering other potential causes.
Consumers should preserve relevant evidence and seek legal advice promptly because statutes of limitations vary by state.
You may have grounds to pursue a product liability lawsuit if medical evidence establishes that the recalled supplement caused or contributed to your heart attack. Attorneys would examine your medical history, supplement use, product identification, and treatment records. A successful claim may allow recovery of medical expenses, lost wages, and other damages permitted by state law.
Potentially. A significant blood pressure increase requiring medical treatment may support a claim if the evidence establishes a connection to the product. Medical records documenting blood pressure readings, symptoms, and treatment can help evaluate causation. The seriousness of the injury and resulting losses are important considerations.
You may still have legal options. Online purchase confirmations, credit card statements, retailer records, photographs, and shipping documentation may help establish that you purchased the affected product. An attorney can evaluate whether sufficient evidence exists to identify the supplement and support an injury claim.
Yes, depending on your circumstances. Consumers who experienced injuries before the recall announcement may still have potential claims. The applicable statute of limitations, evidence of exposure, and medical causation will determine whether a lawsuit can proceed. Prompt legal evaluation is important because filing deadlines vary.
If a death is allegedly connected to a defective supplement, eligible family members or an estate representative may be able to pursue a wrongful death or survival action. State law determines who may file and what compensation may be available. Medical evidence must establish the legally required connection between the supplement and the death.
No. A recall identifies a product safety concern but does not automatically establish that every purchaser has a compensable injury. A personal injury lawsuit generally requires evidence of exposure, injury, causation, and legally recoverable damages. Consumers who suffered significant medical complications should have their circumstances evaluated individually.
Consumers who suffered serious medical complications after using Rapture Pre Workout may have legal options to pursue compensation from companies responsible for defective or dangerous products.
Parker Waichman LLP is a national personal injury law firm representing individuals harmed by unsafe consumer products. Our attorneys can investigate potential claims involving heart attacks, severe hypertension, cardiovascular injuries, and other serious medical complications associated with recalled supplements.
If you or a loved one suffered an injury after using Rapture Pre Workout, call Parker Waichman LLP for a free consultation at 1-800-YOUR-LAWYER (1-800-968-7529). Our legal team can review your circumstances, explain your rights, and determine whether you may have grounds to pursue compensation. Regardless of your location or where your injury occurred, our nationwide product injury law firm is ready to assist you.
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