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Silintan Capsules Recall Injury and Lawsuit Investigation

Silintan Capsules Recalled After FDA Finds a Hidden Prescription Drug Inside

Most drug recalls don’t make headlines until the damage is already done. By the time patients start asking questions, the pattern is clear but the answers are not. The Silintan recall sits squarely in that space. A product once trusted for treatment is now under scrutiny, and for many people, the real issue is no longer what the drug promised but what it may have caused.

If you or someone close to you experienced unexpected complications after using Silintan, you are not alone in trying to connect the dots. Recalls often follow a trail of adverse reports, internal findings, or regulatory concerns that point to a deeper failure in safety or disclosure. What matters now is understanding whether those failures directly contributed to your injury and what legal options may be available.

If you took Silintan capsules for joint or body pain and then suffered a heart attack, stroke, internal bleeding, or kidney failure, the hidden drug inside that supplement may be the reason. You have legal rights, and our firm can help you understand your options.

Our firm has recovered more than $500 million for injured clients across the country. Attorney Matt Wetherington has spent years holding manufacturers and corporations accountable when they sell dangerous or defective products to unsuspecting consumers. We handle Silintan injury and wrongful death cases on a contingency fee basis, which means you pay nothing unless we win.

Call (404) 888-4444 or fill out our quick online form for a free consultation. No fee unless we win.

Official FDA Recall: Silintan Capsules — January 9, 2026

  • Product: Silintan Capsules, sold in 25-count plastic bottles with blue labels
  • Manufacturer: Anthony Trinh, 123Herbals LLC, Rosemead, California
  • Recall Announced: January 7, 2026. FDA Notice published January 9, 2026
  • Reason: Undeclared meloxicam, a prescription NSAID drug, found inside the product
  • Lots Affected: All lot numbers within their expiration dates
  • Distribution: Nationwide through 123herbals.com
  • Legal Classification: Classified as an unapproved new drug under federal law

A Hidden Drug. Real Injuries. And You Had No Idea.

The FDA recall of Silintan capsules is not just a product safety story. It is a personal injury matter for every person who took this supplement without knowing it contained a powerful prescription anti-inflammatory drug. 123Herbals LLC sold a supplement that contained a prescription drug without disclosing it on the label. That drug, meloxicam, carries an FDA black box warning for life-threatening heart attacks, strokes, and gastrointestinal bleeding.

If you or someone you love suffered a serious health event while taking Silintan, you may be entitled to significant financial compensation regardless of where you live in the United States. You do not need to prove that Silintan was the only cause of your injury. You only need to show that it was a contributing factor.

Call (404) 888-4444 or fill out our quick online form for a free consultation. No fee unless we win. There is no cost and no obligation.

What Is Silintan and Who Was Taking It?

Silintan was sold as a natural dietary supplement for joint pain and body aches. 123Herbals LLC distributed it nationwide through its website, 123herbals.com. The product came in blue-labeled plastic bottles with 25 capsules each. At no point did the company disclose that the capsules contained a prescription medication.

People who bought Silintan were looking for relief from chronic joint pain, arthritis symptoms, back pain, and general body aches. Many of these consumers are older adults who also take other medications like blood thinners, diabetes drugs, or blood pressure medications. This matters because meloxicam interacts dangerously with many of those drugs, which makes the risk far greater for this group of patients.

The product was never approved by the FDA as a drug. Under federal law, once a product contains a drug ingredient like meloxicam, it must go through the full FDA drug approval process. 123Herbals LLC bypassed that entirely by labeling the product as a dietary supplement and hiding the drug inside it.

What the FDA Found and Why It Matters

FDA laboratory testing confirmed that Silintan capsules contained meloxicam, a prescription-only nonsteroidal anti-inflammatory drug approved for managing osteoarthritis pain. Because meloxicam was never listed on the Silintan label, the FDA classified the product as an unapproved new drug. That means it was never reviewed or approved for safety or effectiveness. This triggered a voluntary recall of all lot numbers on January 7, 2026.

According to the FDA, exposure to meloxicam above the maximum recommended daily dose of 15 mg creates a real probability of serious, life-threatening events. Those events include blood clots, heart attack, and stroke. The FDA also flagged risks of hypersensitivity reactions, gastrointestinal bleeding, ulceration, intestinal perforation, and acute kidney injury, particularly in elderly patients. People taking blood thinners or other NSAIDs face additional danger from drug interactions that significantly increase bleeding risk.

This Was Not 123Herbals LLC’s First Offense

This recall is not a one-time mistake. In September 2024, 123Herbals LLC recalled another product called Vail-Bon Jie Yang Wan after FDA testing found it contained two other undisclosed prescription drugs: dexamethasone, a powerful corticosteroid, and chlorpheniramine, an antihistamine. That product was sold on Amazon and through the company website nationwide.

The FDA sent 123Herbals a formal warning letter in November 2025 stating directly that Silintan was not the first product the company had sold with hidden drug ingredients. Despite that federal warning, the company continued selling Silintan. This pattern of repeated misconduct strengthens claims for punitive damages, which are available under federal and state product liability laws when a defendant acts with conscious disregard for the safety of others.

How Silintan May Have Harmed You

Meloxicam is a serious prescription drug. When consumed without medical supervision, without proper dosing, and without a doctor who knows a patient is taking it, the risks multiply. The following injuries are directly linked to undisclosed meloxicam exposure. If you experienced any of these while taking Silintan, speak with an attorney right away.

  • Heart Attack: Meloxicam carries an FDA black box warning for increased heart attack risk. This risk applies even to people with no prior heart disease and can occur early in use, not only after months of exposure. If you had a heart attack while using Silintan, you may have a case.
  • Stroke: NSAIDs like meloxicam increase the risk of blood clots that can block arteries in the brain. Strokes caused this way can result in permanent disability, loss of speech, paralysis, or death. Stroke survivors who used Silintan should contact our firm today.
  • Gastrointestinal Bleeding: Meloxicam can cause bleeding, ulcers, and perforation of the stomach or intestines, often with no warning symptoms at all. Signs include black or tarry stools, vomiting blood, or severe abdominal pain. GI bleeding linked to Silintan may be grounds for a lawsuit.
  • Kidney Failure: Meloxicam reduces blood flow to the kidneys. This is especially dangerous for older adults and people already taking diuretics or ACE inhibitors. Acute kidney injury can develop quickly and may require dialysis. Kidney damage after taking Silintan may be compensable.
  • Dangerous Drug Interactions: People taking warfarin, Eliquis, Xarelto, or daily aspirin face a much higher risk of serious bleeding when combined with meloxicam. People using ibuprofen or naproxen at the same time face compounding risks. Drug interaction injuries from Silintan are fully recoverable.
  • Blood Pressure Spikes: Meloxicam can cause significant increases in blood pressure. Uncontrolled high blood pressure damages the heart, kidneys, and blood vessels and can trigger additional cardiovascular emergencies.
  • Liver Injury: Meloxicam has been linked to serious liver damage including fulminant hepatitis and liver failure. Elevated liver enzymes have been reported in patients treated with NSAIDs in clinical trials.
  • Severe Allergic Reactions: The FDA flagged the risk of hypersensitivity reactions from undisclosed meloxicam exposure. These can range from skin rashes to life-threatening anaphylactic reactions requiring emergency medical treatment.

You May Be at Higher Risk If Any of These Apply to You

Not every person who took Silintan will have experienced an injury. But certain groups faced far greater danger based on how meloxicam interacts with specific health conditions and medications. If any of these apply to you and you took Silintan, speak with a doctor and contact our firm.

  • Adults 65 and older, who face heightened kidney and cardiovascular risk from NSAID use
  • People taking blood thinners such as warfarin, Eliquis, Xarelto, or daily aspirin
  • People who also used ibuprofen, naproxen, or other NSAIDs at the same time
  • People with a history of heart disease, prior heart attack, or coronary artery disease
  • People with chronic kidney disease or reduced kidney function
  • People with high blood pressure or on antihypertensive medications
  • People taking SSRIs or antidepressants, which increase bleeding risk when combined with NSAIDs
  • People who recently had surgery, including heart bypass surgery
  • People with a history of stomach ulcers or prior gastrointestinal bleeding
  • People with liver disease or those who drink alcohol regularly

You Had No Way of Knowing What Was in That Bottle

This is the heart of the legal case against 123Herbals LLC. You bought what you believed was a natural supplement for joint and body pain. The label said nothing about meloxicam. You had no reason to tell your doctor you were taking a prescription NSAID, because you did not know you were. You had no way to check for drug interactions, and no information about safe dosing limits.

If you felt side effects while taking Silintan, you probably had no reason to connect them to the supplement. You may have blamed your age, your existing conditions, or other factors. That is exactly what makes this case so serious. The harm was hidden because the drug was hidden. 123Herbals LLC made a deliberate choice to sell a prescription drug inside a supplement label, and that choice caused real people to suffer real injuries.

Under federal product liability law and the product liability statutes of every state, manufacturers are responsible when a defective product they sell causes injury. You do not have to prove the company intended to harm you. You just have to show the product was defective and you were hurt.

Call (404) 888-4444 or fill out our quick online form for a free consultation. No fee unless we win. There is no cost and no obligation.

Wrongful Death Claims Related to Silintan

If your loved one died after taking Silintan capsules and had suffered a heart attack, stroke, gastrointestinal hemorrhage, or organ failure during or after that period, their death may be directly connected to the hidden meloxicam in that product. Families in this situation have the right to pursue a wrongful death claim against the manufacturer.

Wrongful death laws exist in every state in the United States. These laws allow surviving spouses, children, and parents to seek compensation for the loss of a loved one whose death was caused by another party’s negligence or misconduct. In most states, the estate may also pursue a separate survival action covering the medical costs, pain, and suffering the deceased person experienced before passing.

  • Who Can File: Surviving spouses, children, and parents of the deceased may be eligible to file a wrongful death claim in most states.
  • What You Can Recover: Compensation for your loved one’s lost income, loss of companionship, medical costs incurred before death, and in some states the full value of their life.
  • What You Need to Show: A connection between Silintan use and a death caused by a known meloxicam risk such as heart attack, stroke, or internal bleeding.
  • Punitive Damages: Because 123Herbals LLC continued selling Silintan after receiving a formal FDA warning letter, claims for punitive damages may be available to your family.

We understand that no amount of money can replace the person you lost. But holding 123Herbals LLC accountable is how justice works in these cases. It forces companies to change their behavior and provides your family with financial support during an incredibly difficult time.

If your loved one was taking Silintan before they passed, contact us as soon as possible. Deadlines apply to wrongful death claims in every state, and acting quickly helps preserve the evidence that strengthens your case.

Call (404) 888-4444 or fill out our quick online form for a free consultation. No fee unless we win. There is no cost and no obligation.

Do You Have a Silintan Injury Case?

You may have a valid claim if you can answer yes to one or more of the following questions. You do not need to answer all of them. Even partial circumstances may support a strong case.

  • Did you purchase or use Silintan capsules from 123herbals.com or any other retailer?
  • Did you suffer a heart attack, stroke, blood clot, or cardiovascular event while using Silintan?
  • Did you experience gastrointestinal bleeding, stomach ulcers, or intestinal perforation?
  • Were you diagnosed with kidney failure or a significant drop in kidney function?
  • Were you also taking blood thinners, other NSAIDs, or medications that interact with meloxicam?
  • Did your doctor not know you were taking Silintan when treating you for an illness or injury?
  • Did a family member die during or after using Silintan from a cardiovascular or GI event?
  • Did you incur medical bills, miss work, or suffer lasting health effects after using Silintan?

If you answered yes to any of these, contact Wetherington Law Firm today. Our team will evaluate your case at no cost and give you an honest assessment of your options.

What Kind of Lawsuit Silintan Injury Case?

This type of case falls under product liability law, which holds manufacturers responsible when defective products cause injury. You do not have to prove that 123Herbals LLC intended to hurt you. The law in every state requires that companies sell safe, accurately labeled products. When they fail, injured consumers have the right to sue. Here are the specific legal theories that apply to Silintan claims.

  • Product Liability: Manufacturers are strictly liable when a defective product causes injury. Silintan was defective because it contained an undisclosed prescription drug that was never listed on the label.
  • Failure to Warn: The company had a legal duty to disclose all active ingredients, especially a prescription NSAID with known serious risks. They failed entirely to warn consumers about meloxicam.
  • Negligence: 123Herbals LLC acted carelessly by selling a drug-laced supplement and continuing distribution even after the FDA formally warned them in November 2025 about hidden drug ingredients in their products.
  • Fraud and Misrepresentation: The company marketed Silintan as a natural supplement while knowingly including a prescription drug inside it. That is a form of consumer fraud recognized in every state.
  • Punitive Damages: Because this is 123Herbals LLC’s second adulterated product recall and they continued selling Silintan even after an FDA warning letter, courts may award additional punitive damages to punish this conduct.
  • Wrongful Death: If a family member died from injuries caused by Silintan, wrongful death statutes in every US state allow surviving family members to pursue compensation.

Do Not Wait to Contact a Silintan Injury Attorney

Every state has a statute of limitations, which is a legal deadline for filing a lawsuit. In most states, personal injury and product liability claims must be filed within two to three years from the date of your injury. Wrongful death claims follow a similar timeline measured from the date of death. Missing this deadline means permanently losing your right to sue, no matter how strong your case is.

The Silintan recall was announced January 9, 2026. If your injury occurred in 2025 or early 2026, your filing window may already be running. Evidence also becomes harder to preserve as time passes. The sooner you contact our firm, the stronger your case will be.

Call (404) 888-4444 or fill out our quick online form for a free consultation. No fee unless we win. There is no cost and no obligation.

Why Injury Victims Across the Country Trust Wetherington Law Firm

When a company hides a prescription drug inside a supplement and people get hurt, you need a law firm that knows how to go up against corporations and win. Wetherington Law Firm has built its reputation on aggressive, client-focused representation in product liability, personal injury, and wrongful death cases. We represent clients nationwide and have the resources to take on major manufacturers.

  • Over $500 million recovered for clients
  • Available 24 hours a day, 7 days a week
  • No upfront cost to start your case
  • Free case evaluation with no obligation
  • We advance all case expenses — you owe nothing unless we win

Attorney Matt Wetherington personally handles the most complex product liability and wrongful death cases at our firm. Our clients across the country know that when they call us, they get a team that fights hard and does not stop until they get the compensation they deserve.

Call (404) 888-4444 or fill out our quick online form for a free consultation. No fee unless we win. There is no cost and no obligation.

Frequently Asked Questions

Is the Silintan recall real and official? 

Yes. On January 7, 2026, Anthony Trinh, 123Herbals LLC announced a voluntary nationwide recall of all lots of Silintan capsules. The FDA published the official recall notice on January 9, 2026 after its own laboratory confirmed the product contained undeclared meloxicam, a prescription NSAID. The recall covers all lot numbers within their expiration dates, and the product is classified as an unapproved new drug under federal law.

What injuries can meloxicam cause? 

Meloxicam carries an FDA black box warning, the most serious warning the agency issues, for two categories of risk. The first is cardiovascular: blood clots, heart attack, and stroke, which can be fatal and can occur even in people with no prior heart disease. The second is gastrointestinal: bleeding, ulcers, and perforation of the stomach or intestines, which often happen without any warning symptoms. Meloxicam can also cause acute kidney injury, dangerous drug interactions with blood thinners and other NSAIDs, liver damage, and significant blood pressure increases.

How do I know if Silintan caused my injury? 

This is exactly what our legal team helps you determine. Because you did not know you were taking a prescription drug, you likely never told your doctor about it, and your injury may have been blamed on other causes. Our attorneys work with medical experts who review your records and timeline to determine whether your injury is consistent with known meloxicam risks and whether it coincides with your period of Silintan use. You do not have to figure this out on your own.

How much is a Silintan lawsuit worth? 

The value of a case depends on the severity of your injury, your medical expenses, lost income, pain and suffering, and the long-term impact on your life. Heart attack and stroke cases with lasting disability typically carry significant value. Wrongful death cases include the full value of the deceased’s life under applicable state law. Cases that also qualify for punitive damages, which may apply here given 123Herbals LLC’s pattern of repeat offenses, can result in substantially higher awards. We will give you an honest assessment after reviewing your situation.

How long do I have to file a Silintan lawsuit? 

Deadlines vary by state. Most states allow two to three years from the date of injury to file a personal injury or product liability lawsuit. For wrongful death claims, the deadline typically runs from the date of death. Because the recall was announced in early January 2026, if your injury occurred in 2025 or early 2026, your window may already be running. Contact us as soon as possible to protect your right to file.

What does it cost to hire Wetherington Law Firm for a Silintan case? 

Nothing upfront. We handle Silintan injury and wrongful death cases on a contingency fee basis, which means you pay no attorney fees unless we recover compensation for you. We also advance all case costs and expenses. There is no financial risk to you. If we do not win, you owe us nothing.

Can I still file a claim if I did not save the bottle or keep a receipt? 

Yes. While having the bottle or receipt makes documentation easier, you can still pursue a claim without them. Our attorneys can gather purchase history from bank statements, email order confirmations, and medical records that establish the timing of your Silintan use. Do not let the absence of paperwork stop you from reaching out.

Can family members file a wrongful death claim if their loved one died after taking Silintan? 

Yes. Wrongful death laws in every US state allow surviving family members, typically spouses, children, and parents, to file a lawsuit when a loved one’s death is caused by another party’s negligence or a defective product. If the death is connected to Silintan’s hidden meloxicam, including deaths from heart attack, stroke, gastrointestinal hemorrhage, or kidney failure, a wrongful death claim may be available. The estate may also bring a separate action for medical expenses and pain and suffering incurred before the death.

Was 123Herbals LLC warned by the FDA before this recall? 

Yes. The FDA sent 123Herbals LLC a formal warning letter in November 2025 explicitly stating that Silintan was not the company’s first product found to contain hidden drug ingredients. The company had previously recalled Vail-Bon Jie Yang Wan in September 2024, a supplement that contained undisclosed dexamethasone and chlorpheniramine. The FDA’s letter told the company directly that it was their legal responsibility to ensure products they sell do not contain hidden drug ingredients. Despite that warning, Silintan continued to be sold. This history is directly relevant to claims for punitive damages.

The information on this page is for general informational purposes only and does not constitute legal advice. Reading this page does not create an attorney-client relationship. Laws vary by state and your legal rights depend on the specific facts of your case. Past results do not guarantee future outcomes. Contact our firm for advice specific to your situation.

 

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