Pharmaceutical Injuries



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Pharmaceutical Injury Lawyers in Agoura Hills & Westlake Village

We Can Help If You Were Harmed by a Drug or Medical Device

Types of Medical Product Liability Claims

Design Defects

Marketing Defects

Our attorneys have more than 50 years of combined experience helping people like you get what they deserve. We can work with clients on an individual basis or assist in filing a class action lawsuit if the problem is believed to affect many more people.

Millions of Americans rely on medications and medical devices to treat serious health conditions. Unfortunately, in some cases, severe adverse side effects can lead to a host of new problems for the patient. While it is impossible to guarantee absolute safety when it comes to drug effects and medical devices, in some cases the drug or device maker may have known about certain adverse side effects but failed to disclose the risk to medical professionals or the public.

If you suffered adverse side effects from a drug or medical device, you may be eligible to file a drug injury lawsuit to seek payment for your injuries. At Bradley/Grombacher, we can help people like you seek fair and just compensation when a drug you are taking or medical device you are using has caused injury.

In some cases, the manufacturer or other affiliated company provides consumers with inadequate warnings or inadequate instructions about how to use the product. Some manufacturers fail to warn consumers and medical professionals about the foreseeable risks of using a product.

A design defect is a product liability claim that refers to cases in which it is foreseeable that a drug or medical device will cause injury because of its design. If the drug maker is aware that the drug could be dangerous, it has a responsibility to conduct extra studies or reconfigure the product to avoid or reduce the risk of injury.

In these cases, the manufacturer or another negligent party could be held liable if a person suffers a foreseeable side effect.

Sometimes mistakes occur during the manufacturing process that can cause a product to be defective and potentially cause harm to a consumer. Once the manufacturer becomes aware that a manufacturing defect has occurred, it has a responsibility to notify consumers and may decide to recall the product over safety concerns.

Manufacturing Defects

If you or a loved one has experienced an adverse reaction from a drug or medical device, you may have a legal claim. The pharmaceutical injury lawyers in Agoura Hills and Westlake Village at Bradley/Grombacher LLP can help you evaluate your claim and move forward with it to seek fair and just compensation.

Let Us Help You With Your Drug Injury Claim

Plaintiffs who have been injured by a medical device defect or a dangerous drug may be eligible to file a product liability or personal injury lawsuit. There are three types of product liability cases: design defects, marketing defects, and manufacturing defects.

Drugs & Medical Devices Under Investigation

Below is a list of drugs and medical devices facing allegations for defects that have seriously injured patients:

  • Xarelto - Xarelto is a new-generation blood thinner that has been linked to serious and life-threatening bleeding incidents without an antidote to limit bleeding damage.


  • IVC Filter - Inferior Vena Cava Filters, or IVC Filters, are small web-like devices implanted in the in vein of patients at risk of blood clots, which may lead to damage such as a pulmonary embolism. However, these devices have been linked to migration, vein penetration, and fracture, leading to serious complications.


  • Physiomesh (hernia mesh) - Physiomesh is a hernia mesh product made by Ethicon, a Johnson & Johnson company. These hernia mesh products are allegedly linked to adhesions, obstructions, migration, infections, and hernia recurrence.


  • Talc Powder (baby powder) - Talc powder is used in common products such as baby powder and cosmetics, but this common product has also been linked to ovarian cancer.


  • Essure - Essure is a non-surgical permanent birth control option that is less invasive than tubal ligation, but several Essure patients report that they have suffered serious pain, bleeding, organ perforation, miscarriage, ectopic pregnancies, and unwanted pregnancies.


  • Fluoroquinolone Antibiotics - Several common antibiotics have been linked to aortic aneurysms and aortic dissections. The antibiotics linked to these side effects include Avelox, Levaquin, and Cipro.


  • Hip Implants - Several metal-on-metal hip implants have been linked to serious side effects including hip implant failure, hip dislocation, metal poisoning, cancer, and tissue death.


  • Shoulder Implants - Shoulder implants have been linked to a high fracture rate, metal toxicity, bone and tissue damage, erosion, and dislocation.


  • Invokana - The diabetes drug Invokana has been linked to serious side effects such as kidney failure and ketoacidosis.


  • Heartburn Drugs - A class of heartburn medications known as proton pump inhibitors (PPIs) allegedly increase the chance of developing chronic kidney disease and an increased risk of a heart attack or heart failure. PPI heartburn drugs include Nexium, Prilosec, Prevacid, Dexilant, Protonix, and Aciphex.

Types of Drug Injuries

Drugs are designed to treat a wide variety of health conditions. Therefore, drug side effects widely vary based on the type of drug and an individual’s reaction to it. Some common side effects of drugs include nausea, gastrointestinal issues, skin reactions, drowsiness, and antibiotic rash.



The manufacturers of drugs and medical devices are required to list the common medication side effects associated with the product on the product’s label. This information allows a consumer to know if the drug side effects they are experiencing are normal or if medical attention is necessary. Failure to seek medical attention for dangerous prescription side effects may lead a person to suffer a catastrophic drug injury, which may have lifelong effects and diminish a person’s quality of life.


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Find Out How to File a Defective Medical Product Lawsuit

If you or a loved one has suffered a medical device injury or dangerous drug side effect, you may qualify to file a drug injury lawsuit. You may be entitled to compensation for your medical bills, pain and suffering, lost wages, and other damages you experienced as a result of the drug or medical device problems.

Contact the pharmaceutical injury attorneys in Agoura Hills and Westlake Village at Bradley/Grombacher LLP to discuss your legal options. If you have a potential case, your defective drug lawyer will work tirelessly on your behalf to put together a compelling case and help you get the compensation you deserve.

Galvan v. Doe

$6,750,000

Who Is Responsible for Drug Safety?

The U.S. Food and Drug Administration (FDA) regulates drugs and medical devices. This federal agency is responsible for evaluating medications and medical devices for their safety and efficacy. The FDA also may choose to approve a drug or medical device only to treat specific conditions. The approved conditions and safety risks are listed in the safety information that accompanies the drug or medical device.

Physicians who opt to use the drug to treat any unspecified condition are prescribing the drug for “off-label” use. While physicians are permitted to prescribe drugs for an off-label use, drug makers are not allowed to promote the drug for an off-label use. Drug manufacturers are only allowed to promote their drugs to treat illnesses for which the FDA approved them.

Drug and medical device manufacturers have a duty to ensure that their products are safe and that they comply with FDA regulations before they put the products on the market. Medical devices and drugs must be thoroughly and reliably tested to ensure their safety and efficacy before they can be approved to enter the market, and they must disclose all test results with the FDA.



If they fail to do so, drug and medical device makers may be subject to legal liability.


By Grombacher April 20, 2026
Trajector Faces Class Action Lawsuit Over Alleged Deceptive and Abusive Practices Toward Nation’s Disabled Veterans Los Angeles, CA – April 15, 2026 - Bradley Grombacher filed a nationwide class action lawsuit in Federal court alleging Trajector, Inc. and Trajector Medical, LLC engaged in a widespread scheme to unlawfully charge disabled veterans for assistance with Department of Veterans Affairs (VA) disability claims. According to the complaint, federal law strictly regulates who may assist veterans with preparing, presenting, or prosecuting VA disability claims. Only VA-accredited attorneys, agents, or representatives may provide such services for compensation, and no fees may be charged for assistance with an initial claim. The class action lawsuit alleges that the defendants ignored these requirements entirely, operating without accreditation while charging veterans thousands of dollars, often between $4,500 and $20,000, for services that were either prohibited or required to be free. “Our nation owes its freedom to those brave enough to serve, and Trajector took advantage of these people, violated the law, and continues to prey upon new victims daily,” said attorney Kiley Grombacher of Bradley Grombacher. The complaint further alleges that the defendants’ business model relied on deceptive marketing and misleading contracts that obscured the true nature of their services and fees. Veterans were led to believe they were receiving legitimate assistance designed to maximize their disability ratings. In reality, the plaintiffs claim the Trajector performed tasks that constitute regulated “representation,” including gathering medical records, completing forms, and advising on claim strategy, and all without legal authority. A central component of the alleged scheme involved the use of an automated system known as “CallBot,” which accessed VA systems using veterans’ personal information to monitor changes in their disability benefits. Once a benefit increase was detected, the Trajector issued invoices calculated as a multiple, often five times, of the veteran’s monthly benefit, regardless of whether the company contributed to the outcome. The plaintiffs also allege that the defendants employed aggressive and abusive collection tactics, including repeated phone calls, threats of legal action, and persistent demands for payment, even when the charges were disputed. These practices, the complaint asserts, caused significant financial harm and emotional distress, particularly given the vulnerability of disabled veterans. The case is Gilbert Quijada, Jr. v. Trajector, Inc., USDC Central District of California – Western Division, Case No. 2:26-cv-03792.
By Grombacher April 20, 2026
Bradley/Grombacher Partner Kiley Grombacher Named to Daily Journal’s 2026 List of Leading Commercial Litigators Westlake Village, California – The Daily Journal named Bradley/Grombacher partner Kiley Grombacher to its 2026 list of Leading Commercial Litigators, recognizing her leadership in high-stakes class actions and mass tort litigation and her work holding corporations accountable in complex consumer, workplace, and product safety cases. Grombacher has built her practice around representing individuals harmed by corporate misconduct, with a focus on nationwide class actions, multidistrict litigation, and cases involving toxic exposure, defective products, and workplace rights. She regularly takes on well-funded defendants in cases that turn on scientific evidence, internal corporate records, and regulatory history. “I’ve always been driven by the simple goal to hold powerful institutions accountable and give people a meaningful path to justice,” Grombacher said. “This recognition reflects the work our team puts in every day to take on complex cases that can create real change.” Among her most notable matters, Grombacher served as lead counsel in nationwide litigation involving Neutrogena aerosol sunscreen products found to contain benzene, a known carcinogen. The case resulted in a class settlement that provided compensation and product vouchers to consumers while drawing national attention to product safety and labeling practices. She also holds a leadership role in ongoing multidistrict litigation challenging the marketing of over-the-counter medications containing phenylephrine. Plaintiffs allege manufacturers promoted the ingredient as an effective nasal decongestant despite longstanding evidence that it is ineffective when taken orally. In addition to consumer cases, Grombacher represents workers in high-impact litigation involving environmental and workplace exposure. She currently advocates for individuals who allege they suffered harm after exposure to hazardous substances, including lead and asbestos, at the Goodfellow Federal Complex in St. Louis. The Daily Journal’s annual list highlights attorneys who lead complex commercial litigation matters across the country, often involving cutting-edge legal theories, extensive evidentiary records, and significant public impact. Grombacher said her work reflects broader shifts across the legal landscape. “We’re seeing increased scrutiny of product safety, corporate transparency, and workplace conditions,” she said. “Litigation plays a critical role in setting standards that protect both consumers and employees.” Grombacher practices out of Bradley/Grombacher’s Westlake Village office and has spent nearly two decades litigating complex cases nationwide. About Bradley/Grombacher Bradley/Grombacher is a plaintiff-side law firm focused on complex litigation, including class actions, mass torts, consumer protection, and employment matters. The firm represents individuals and groups in high-impact cases against corporations and institutions across the country.

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