Know Your Rights About Filing a Clonazepam Lawsuit

In November 2024, thousands of patients and families across the United States were shocked to learn about a significant recall involving a widely prescribed anxiety medication: Clonazepam, also known by its brand name, Klonopin. Individuals across the country are filing clonazepam lawsuits.

The recall, announced by Endo, Inc.—the drug manufacturer of the orally disintegrating Clonazepam tablets—was prompted by a dangerous mislabeling issue that put patients at risk of accidental overdose.

If you or a loved one has experienced severe side effects or adverse reactions after taking recalled Clonazepam Orally Disintegrating Tablets, you may be eligible to file a Clonazepam lawsuit and pursue compensation for your injuries.

At The Yost Legal Group, our experienced product liability attorneys are dedicated to holding pharmaceutical companies accountable and ensuring that victims receive the justice and support they deserve.

In this blog, we’ll break down what happened with the Clonazepam recall, the potential dangers, how to file a product liability claim, and how The Yost Legal Group can help.

Know Your Rights About Filing a Clonazepam Lawsuit

What Is Clonazepam (Klonopin)?

Clonazepam is a prescription medication commonly used to treat anxiety disorders, panic attacks, and certain types of seizures.

As a benzodiazepine, Clonazepam works by calming the brain and nerves, making it a trusted option for millions of patients who rely on it for daily symptom management.

Klonopin, the brand name version, is well-known for its efficacy and is often prescribed in both standard and orally disintegrating tablet (ODT) forms.

Details of the 2024 FDA Clonazepam Recall

In November 2024, Endo, Inc. announced a voluntary recall of specific lots of Clonazepam Orally Disintegrating Tablets (ODT) after discovering a serious labeling error.

According to the FDA’s official recall notice, the outer packaging of certain Clonazepam ODT products listed a lower dosage than what was actually contained in the blister packs.

In other words, patients who believed they were taking a lower, doctor-recommended dose may have inadvertently ingested a much higher amount of the drug.

Example of the Mislabeling Issue

Imagine receiving a prescription labeled as 0.5 mg tablets, only to discover the actual blister packs inside contain 2 mg tablets—a fourfold increase in dosage.

For patients with anxiety or seizure disorders, this discrepancy can have life-threatening consequences.

Why Is the Mislabeling of Clonazepam so Dangerous?

Benzodiazepines like Clonazepam are potent medications. Even small increases in dosage can cause:

–             Severe drowsiness or sedation

–             Confusion and impaired coordination

–             Respiratory depression (slow or shallow breathing)

–             Risk of overdose, especially in elderly patients or those with other health conditions

For some, accidental overdose can lead to hospitalization, long-term health complications, or even death.

Who Is Affected by the Clonazepam Recall?

The recall specifically involves certain lots of Clonazepam Orally Disintegrating Tablets manufactured by Endo, Inc.

If you or your loved one filled a prescription for Clonazepam ODT in late 2024, it’s critical to check whether your medication is part of the recall.

How to Check Your Medication:

Visit the FDA’s recall page here for a complete list of affected lot numbers and photos of the recalled packaging.

–             Compare the lot number on your medication’s blister pack to those listed by the FDA.

–             If you find a match, stop taking the medication immediately and contact your healthcare provider for guidance.

Risks and Injuries from Taking a Higher-Than-Recommended Dose of Clonazepam

The mislabeling of Clonazepam Orally Disintegrating Tablets is not just a paperwork error—it’s a potentially life-altering or life-threatening mistake.

When patients unknowingly take a much higher dose of Clonazepam than their doctor intended, the risks go far beyond mild side effects. The consequences can be severe and sometimes catastrophic.

Severe Drowsiness and Sedation

Clonazepam is a powerful sedative, and even at prescribed doses, it can cause drowsiness. But when the dose is accidentally multiplied, the sedative effects can become overwhelming. Patients may experience:

–             Extreme fatigue

–             Inability to stay awake

–             Difficulty responding to their environment

Real-World Impact:

Severe drowsiness and sedation dramatically increase the risk of motor vehicle accidents.

A person who takes a higher dose than intended may feel too tired to drive safely, react slowly to hazards, or even fall asleep at the wheel.

This can result in putting not only the patient but also passengers, other drivers, and pedestrians at risk.

–             Rear-end collisions

–             Running off the road

–             Causing multi-vehicle accidents

Falls, Traumatic Brain Injuries, and Broken Bones from Clonazepam Overdose

The sedative effects of Clonazepam can also lead to loss of balance and falls, especially in older adults or those with existing mobility issues. A sudden, unexplained fall can cause:

–             Traumatic brain injuries (TBI)

–             Concussions

–             Broken hips, wrists, or other bones

–             Internal bleeding

These injuries often require emergency medical care, surgery, and long-term rehabilitation. In some cases, the consequences can be permanent or even fatal.

Confusion and Impaired Coordination

A higher-than-recommended dose of Clonazepam can cause profound confusion, memory problems, and impaired coordination. Patients may become disoriented, unable to follow instructions, or struggle to perform everyday tasks.

Who Is Affected by the Clonazepam Recall

Workplace Dangers from Clozazapan Overdose

For individuals who operate vehicles, heavy equipment, or machinery as part of their job, these symptoms can be especially hazardous. Confusion and poor coordination can lead to:

–             Driving errors, causing serious or fatal crashes

–             Mishandling of industrial equipment, resulting in workplace accidents

–             Dropping heavy objects or tools, risking injury to themselves or coworkers

–             Respiratory Depression and Life-Threatening Overdose

In the most severe cases, taking too much Clonazepam can slow breathing to dangerously low levels—a condition known as respiratory depression. Without prompt medical intervention, this can lead to loss of consciousness, brain damage, or death.

Steps to Take if You Took The Mislabeled Clonazepam

Seek Medical Attention: If you are experiencing symptoms of overdose or any unusual side effects, seek medical help immediately.

Preserve Your Medication: Do not throw away the recalled tablets or packaging. These can serve as critical evidence in a potential lawsuit.

Document Everything: Keep a record of your symptoms, medical visits, and any correspondence with your pharmacy or healthcare provider regarding the recall.

Contact a Product Liability Attorney: Legal professionals can help you understand your rights and the next steps for pursuing compensation.

Legal Rights: Can You File a Clonazepam Lawsuit?

Pharmaceutical companies have a legal duty to ensure their products are safe and accurately labeled.

When a company fails to meet this obligation, and patients are harmed as a result, victims have the right to seek justice through a product liability lawsuit.

You may have a valid Clonazepam Overdose claim if:

–             You or a loved one took the recalled Clonazepam ODT and experienced adverse effects

–             The medication you received was part of the recalled lots

–             You suffered physical, emotional, or financial harm as a result

–             Potential compensation in these cases can cover:

–             Medical expenses (hospitalization, doctor visits, medications)

–             Lost wages due to missed work

–             Pain and suffering

–             Long-term health impacts

–             Wrongful death (in tragic cases involving fatal overdoses)

How The Yost Legal Group Can Help

At The Yost Legal Group, our mission is to advocate for individuals and families harmed by dangerous or defective medications. We understand the fear and frustration that come with medication recalls and unexpected health crises.

Our experienced attorneys for defective products have successfully represented clients in complex pharmaceutical litigation nationwide.

What We Offer:

Free, Confidential Consultation: We’ll review your case, answer your questions, and explain your legal options at no cost.

Contingency Fee Representation: You pay nothing unless we win compensation for you.

Compassionate Support: Our team is dedicated to providing personalized, respectful service every step of the way.

If you believe you have a Clonazepam lawsuit, don’t wait. Evidence can disappear, and strict legal deadlines may apply.

Contact our Defective Drug Lawyers Today

If the Clonazepam recall has negatively impacted you or a loved one, you deserve answers, accountability, and compensation for your suffering. The Yost Legal Group is here to help.

Contact our product liability lawyers today to schedule your free consultation:

Phone: (800)-YOST-LAW or (866)-841-4597

Text: 1-410-659-6800

Website: www.yostlaw.com

Let us help you protect your rights and pursue the justice you deserve.

Resources:

FDA Recall Notice: Endo Expands Voluntary Recall of Clonazepam Orally Disintegrating Tablets

Final Thoughts

Medication errors can have devastating consequences, but you are not alone. With an experienced pharmaceutical liability lawyer, you can hold negligent manufacturers accountable.

This will help secure a safer future for yourself and your loved ones. If you have questions or need help navigating your next steps, The Yost Legal Group is just a call or text away. Please continue to check our website for Clonazepam overdose updates.

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Clonazepam Recall Law Firm – Clonazepam Injuries – Defective Product Lawyers

Are You Affected by the Clonazepam Recall?

The FDA Food and Drug Administration has issued a recall for 16 lots of Clonazepam manufactured by Endo, Inc., following a critical labeling error. The product safety recall is hoping to prevent medication errors.

According to the safety alert, the strength listed on the product cartons (0.125 mg) did not match the actual strength of the tablets inside (0.25 mg).

This discrepancy means the tablets were 100% stronger than what patients were led to believe. The wrong Clonazepam dose poses significant health and safety risks for individuals taking the medication.

Clonazepam Recall Lawsuit for mislabeling drug dosage

Clonazepam Recall Lawsuits: What You Need to Know Now

In an official statement, Endo shifted the blame for this mishap onto a “third-party packager”:

“The product … is being recalled due to mislabeling where an incorrect strength appears on the cartons … due to an error at a third-party packager.”

But Endo hired this company. And the product belongs to Endo. Therefore, this is their responsibility to bear, as it puts thousands of people at risk of overdosing on its drug.

Given the recall, the FDA agrees. And with that safety warning, The Yost Legal Group has taken action to represent people harmed by the potentially deadly mislabeling.

If you or a loved one has suffered an adverse reaction due to the mislabeling of Clonazepam, The Yost Legal Group is here to help.

Patient Risks for Taking Mislabeled Clonazepam Medication

FDA Recalls Clonazepam Drug for Safety Concerns

With over 30 years of experience in representing victims of accidents caused by negligence, our defective drug attorneys will provide compassionate and experienced support as you seek the justice you deserve.

Pharmaceutical errors are unacceptable, and we believe in holding Big Pharma accountable for its mistakes.

Contact The Yost Legal Group product liability lawyers today for a free consultation. Call 1-800-967-8529 to speak with our caring and experienced legal team.

Clonazepam: The Generic Name for Klonopin

The brand name for Clonazepam is Klonopin, which is more widely recognized by the general public. However, it is essential to note that any potential litigation against Endo, Inc. regarding the mislabeling of its product applies only to Clonazepam, not to other products.

Klonopin is a brand name owned by a different company. Clonazepam is the generic name. There are also several other manufacturers of Clonazepam, but they are not relevant to this potential litigation.

We are only focusing on Endo’s version of the drug, as that is, to this point, the only version that was distributed with the potentially harmful mislabeling.

FDA Recalls Clonazepam Drug for Safety Concerns

What Is Clonazepam?

Clonazepam is a generic medication belonging to the benzodiazepine class of depressant drugs. That is a fair amount of pharmaceutical jargon and terminology, so let’s break it down piece by piece.

  • Depressants: You are probably familiar with depressant drugs. As a slang term, they are often referred to in casual conversations as “downers.” These types of drugs affect the brain’s activity.

They slow neurotransmission levels and decrease electrical activity in the brain. Depressants also inhibit an individual’s ability to feel arousal and stimulation.

While this might sound negative, this reduction in brain activity is precisely why depressant drugs can be effective when used correctly by the discretion of a medical professional to relieve disorders and symptoms such as various anxiety disorders, depression, insomnia, obsessive-compulsive disorder, and seizures.

Alcohol, benzodiazepines, and cannabis are some of the most common types of depressant drugs.

  • Benzodiazepines: As mentioned above, benzodiazepines, known colloquially as “benzos,” are a class of depressant drugs. This type of drug derives its name from its chemical compound, which is a fusion of a benzene ring and a diazepine ring.

Medically, benzodiazepines are used to treat anxiety and panic disorders, insomnia, and seizures.

Common types of benzodiazepines include alprazolam (Xanax®), clonazepam (Klonopin®), and diazepam (Valium®).

Mislabeling Medication Could Affect Your Safety

Clonazepam and benzodiazepines, in general, are often used to treat anxiety disorders, bipolar mania, and seizures as their structural formulae target certain receptors in the brain (GABAA) to produce a calming effect, thus reducing anxiety, preventing seizures, and promoting relaxation.

People living with conditions such as anxiety, bipolar disorders, or epilepsy depend upon their medicine to help them get through their days. Their medications are vital to their mental and physical health.

Now, with Endo’s labeling error, which the company itself has referred to as “possibly life-threatening” in the FDA safety warning, some patients may lose confidence or trust in the medication that helps them manage their condition.

If you or someone you care about has been affected by a defective drug or Endo’s Clonazepam due to a labeling error, you may be eligible for compensation.

Contact the skilled defective drug attorneys at The Yost Legal Group for a free, confidential consultation.

Protecting your health and well-being is important, so don’t wait. Call 1-800-967-8529 now to learn more.

Side Effects of Clonazepam

Even when taking a benzodiazepine such as Clonazepam in the appropriate doses and dosage, there is still the potential for adverse effects because of the change to the brain’s chemical composition.

The most common side effects of Clonazepam include the following:

  • Depression
  • Dizziness
  • Drowsiness
  • Fatigue
  • Forgetfulness
  • Lack of coordination

Know Your Rights After Endo’s Labeling Error

If one has taken a dose that is 100% higher than what a doctor has prescribed because the labeling on the packaging lists an incorrect strength, these side effects become much more harmful and potentially deadly.

Overdosing on benzodiazepines like Clonazepam or combining them with opioid medications can lead to profound sedation that is hard to wake from, respiratory depression that can lead to suffocation, coma, and, in the absolute worst case, death.

Endo must be held responsible for its mistake, even if it plans to shift the blame to the third-party packager that printed and applied the labels. After all, it was Endo who hired the third-party packager in the first place.

Furthermore, as previously stated, there are several manufacturers of Clonazepam. Endo is not alone in the production of this benzodiazepine.

However, Endo is the only company to have its version of Clonazepam recalled by the FDA. And if people have been harmed, we will help them hold the company to account.

Patient Risks for Taking Mislabeled Clonazepam Medication

A two-fold overdose of Clonazepam poses serious risks for children and adults. Potential adverse effects include:

–             Significant sedation

–             Dizziness

–             Ataxia

–             Confusion

There is also a considerable likelihood of severe and potentially life-threatening respiratory depression. This risk increases for individuals with:

–             Pulmonary disease

–             Those prescribed near-maximal dosing

–             Those taking other medications that may contribute to respiratory depression

Your Health May Be at Risk After a Drug Recall

To check if your Clonazepam is affected by a recall, follow these steps:

  • Check your packaging

Look for the lot number on the carton of your Clonazepam product.

  • Compare the lot number.

Visit the FDA website for the complete list of recalled lot numbers. Or check the list below. Endo USA, Inc. is recalling certain Clonazepam Orally Disintegrating Tablets due to potential mislabeling of the carton strength.

  • Contact your healthcare provider or pharmacy.

If your lot number matches one on the recall list, reach out to your healthcare provider or the pharmacy that dispensed the medication for next steps.

Taking these precautions is essential for ensuring the safety and appropriateness of your medication.

Lots Affected by the Clonazepam Recall

Potential Product Description / NDC Number 

Lot Number Expiry Date

Clonazepam ODT, USP (C-IV) 2mg / 49884-310-02

550176501 Feb 2027

550176601 Feb 2027

Clonazepam ODT, USP (C-IV) 0.125mg / 49884-306-02

550174101 Jan 2027

Clonazepam ODT, USP (C-IV) 0.25mg / 49884-307-02

550142801 Aug 2026

550142901 Aug 2026

550143001 Aug 2026

550143101 Aug 2026

550143201 Aug 2026

550143301 Aug 2026

550143401 Aug 2026

550147201 Aug 2026

550147401 Aug 2026

Clonazepam ODT, USP (C-IV) 1mg / 49884-309-02

550145201 Aug 2026

550175901 Feb 2027

550176001 Feb 2027

550176201 Feb 2027

According to ClinCalc.com, Clonazepam was the 57th most prescribed drug in the United States in 2022. In 2022, more than 11.5 million prescriptions of Clonazepam were distributed to nearly 2 million patients.

Fight Back Against Medication Risks, Protect Your Rights

This mislabeling potentially puts millions of people at risk. While it is true that Endo has acknowledged the error and acknowledged the risk (as evidenced by their “possibly life-threatening” quote), its claim that there have been no reports of adverse events rings hollow.

Defective Drug Lawyers Protecting Your Rights

The Yost Legal Group is representing clients harmed by Clonazepam overdose from mislabeled packaging. If you have experienced serious side effects or if a loved one has died from an overdose due to this mislabeling error, call us for help.

We handle cases involving medication errors, FDA pharmaceutical recalls, and recalled drugs. If a prescription medication like Clonazepam tablets caused you harm, contact our drug recall lawyers.

If a defective drug has harmed you or a loved one, contact The Yost Legal Group today. Our experienced defective drug lawyers will immediately begin working on your case. We will help you understand your rights and seek the compensation and justice to which you are entitled.

Every consultation is free, and there are no fees unless we win your case.

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FDA Announces Voluntary Clonazepam Recall

The Benzodiazepine, a Generic Form of Klonopin, Had a “Life-Threatening” Labeling Error

A vital safety alert was issued for Clonazepam users. Endo, Inc., a pharmaceutical company based in Pennsylvania, has recalled its seizure medication, Clonazepam tablets.

The recall is due to a mistake in labeling the product strength on the carton. Such a serious error could lead to life-threatening consequences for thousands of users.

The recall is part of an FDA investigation. Endo, Inc. expanded its initial voluntary recall from July 16. The FDA announced the expanded recall in an alert on Nov. 19.

Clonazepam pillss recalled from the market

Urgent Warning for Clonazepam Users—Verify Your Dose Now

If you use clonazepam benzodiazepine, check your product’s labeling immediately. People who take a higher dose of Clonazepam could face serious health risks, including:

–      Extreme drowsiness

–      Confusion

–      Dizziness

–      Slowed reflexes

–      Lack of coordination

–      Low muscle tone

–      Life-threatening respiratory depression

There is a significant chance of life-threatening respiratory depression:

  • Particularly for individuals with lung conditions
  • Those already prescribed high doses of Clonazepam
  • Patients taking other medications that suppress breathing

If you have experienced a severe adverse reaction from Clonazepam, contact 1-800-967-8529 for a 100% Free and Confidential consultation. The Yost Legal Group is a highly experienced Product Liability law firm. Our Clonazepam lawyers will investigate what happened and fight to seek the justice and financial compensation you deserve.

 Clonazepam can cause adverse reactions

What Is Clonazepam?

The drug Clonazepam is a generic drug under the benzodiazepine class of depressant drugs.

Depressants: These types of drugs affect the brain’s activity. They slow neurotransmission levels and decrease electrical activity in the brain. Depressants also inhibit an individual’s ability to feel arousal and stimulation.

This reduction in brain activity is why depressant drugs can be effective when used correctly. A medical professional prescribes them to relieve disorders and symptoms such as:

  • Anxiety disorders
  • Depression
  • Insomnia
  • Obsessive-compulsive disorder
  • Seizures

Alcohol, benzodiazepines, and cannabis are some of the most common types of depressant drugs.

Benzodiazepines: Benzodiazepines, known as “benzos,” are a class of depressant drugs. This type of drug derives its name from its chemical compound, which is a fusion of benzene and diazepine rings.

Medically, benzodiazepines are most often used to treat anxiety and panic disorders, insomnia, and seizures. Common types of benzodiazepines include alprazolam (Xanax®), clonazepam (Klonopin®), and diazepam (Valium®).

Clonazepam is a generic benzodiazepine sold under the brand name Klonopin®, which more people are probably familiar with. This recall, however, pertains only to the generic version.

Clonazepam side effects, file a Clonazepam lawsuit

Severe Health Risks Linked to Incorrect Clonazepam Dosage

Clonazepam is often used to treat anxiety disorders, bipolar mania, and seizures. Anyone with these ailments and conditions needs regular help. For some people, it might be difficult to make it through a day without their prescribed medication.

Pharmaceutical companies have a clear duty to ensure their products are safe. This includes items people apply, ingest, or inject. They must also make sure their product labels are accurate. These labels tell people how to use their medications safely.

The recall for Clonazepam relates to the tablet version, as the drug is most often taken orally.

The packaging had a labeling mistake. The company said it was “possibly life-threatening.” This was also noted in the FDA safety warning. If a user took the wrong amount of the medication, it could be dangerous. This happened because the number of milligrams in each tablet was incorrect.

If you or someone you know may have been affected, seek medical attention immediately. Contact The Yost Legal Group’s “Dangerous Drugs” division to learn about your legal rights.

Life-Threatening Clonazepam Risks—Know Your Legal Rights

This was no small mistake. In 1960, Clonazepam was patented and became available in the United States in 1975. Doctors have prescribed the drug often since it has been on the market for decades.

According to ClinCalc.com, Clonazepam was the 57th most prescribed drug in the United States in 2022. More than 11.5 million prescriptions of Clonazepam were made out to nearly 2 million patients in 2022.

This mislabeling put millions of people at risk. Furthermore, it was not the first time Endo was derelict in its duties regarding labeling its clonazepam packaging.

The product recall focuses on Clonazepam drug side effects, one of which can result in death from Clonazepam. The product liability lawyers at The Yost Legal Group are here to help. Many FDA recalls exist; the highest level occurs when the FDA issues an FDA Black Boxed Warning. This usually happens when a company is about to remove a drug from the market.

The First Clonazepam Recall of 2024

On July 17, 2024, the FDA published a safety alert that it voluntarily recalled many orally disintegrating drugs due to mislabeling.

Endo announced that the lot it was recalling included packaging that under-reported the strength of each tablet:

“The product lot [550147301] is being recalled due to mislabeling where an incorrect strength appears on the cartons of some packs to show the product strength as 0.125 mg and not 0.25 mg due to an error at a third-party packager.”

Regardless of the mistake by the “third-party packager,” Endo bears responsibility as the drug manufacturer and the employer of the company that packages its medication.

However, it was just one lot and one recall. As Endo noted in its statement, “to date [the company] has not received any reports of adverse events associated with this product lot recall.”

But it would not remain just one lot and one recall for much longer.

If a defective drug harmed you or a loved one, you may have a case and be entitled to compensation. Call or text the experienced defective drug lawyers at The Yost Legal Group today for a free consultation: 410-659-6800.

The Second Clonazepam Recall of 2024

As previously stated, Endo voluntarily recalled Clonazepam in November 2024, and the FDA ran a safety alert. The second recall, however, was not just to announce the recall of a second lot. The alert included a whopping 16 lots of the drug.

The table below includes the product description (Clonazepam Orally Disintegrating Tablets), the National Drug Code number, and the lot number.

Potential Product Description / NDC Number  Lot Number Expiry Date

Clonazepam ODT, USP (C-IV) 2mg / 49884-310-02 550176501 Feb 2027

550176601 Feb 2027

Clonazepam ODT, USP (C-IV) 0.125mg / 49884-306-02 550174101 Jan 2027

Clonazepam ODT, USP (C-IV) 0.25mg / 49884-307-02 550142801 Aug 2026

550142901 Aug 2026

550143001 Aug 2026

550143101 Aug 2026

550143201 Aug 2026

550143301 Aug 2026

550143401 Aug 2026

550147201 Aug 2026

550147401 Aug 2026

Clonazepam ODT, USP (C-IV) 1mg / 49884-309-02 550145201 Aug 2026

550175901 Feb 2027

550176001 Feb 2027

550176201 Feb 2027

Again, Endo placed the blame on its third-party packager:

“Endo’s ongoing investigation has identified the possibility that the Clonazepam product lots listed below contain a limited number of cartons printed with the incorrect strength and National Drug Code (NDC) code due to an error by a third-party packager.”

Serious Side Effects from Clonazepam? We Can Help

Endo is responsible for its medication, and for the third-party packager/s, it hires to label its products. Although the actual medication is not defective, it is still vital to ensure the labeling is correct so that people using the drug can do so safely.

This repeat of negligence with mislabeling puts real people at risk. As of 2022, nearly 2 million people were prescribed Clonazepam, and now there are 16 recalled lots. Endo put its customers in harm’s way.

We do not know how the packages got the wrong information. However, we have seen how small details can be missed at big pharmaceutical companies. Some companies cut corners to save money, which harms people. The result is almost always putting innocent people at risk.

Clonazepam Adverse Reaction? Seek Justice Today

The Yost Legal Group has a long history of representing individuals and their families after a defective drug altered someone’s life.

Drug companies are billion-dollar multinational corporations with some of the best pharmaceutical lawyers in the world. A skilled and experienced defective drug lawyer must handle the complex legal issues when suing a Big Pharma company.

That is where The Yost Legal Group’s accomplished defective drug lawyers factor into the equation. As leading personal injury attorneys, we file product liability lawsuits every day. Let us file your Clonazepam claim.

Many cases involve prescription drugs because of “failure to warn” and “serious pharmaceutical side effects.”

If a defective drug has harmed you or a loved one, please get in touch with The Yost Legal Group today. Our defective drug lawyers will start working on your case right away. They will help you understand your rights to seek the compensation and justice you deserve. Call or text us at 410-659-6800.

All consultations are free, and you do not owe us anything unless we take on and win your case.

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