Defective drug and medical device cases are handled as mass torts — large groups of similar claims coordinated across courts to allow individual victims to pursue justice efficiently. Cellino Law has experience navigating multidistrict litigation (MDL) proceedings, state court mass tort coordination, and the complex expert testimony that these cases require.
Call Cellino Law today for a free defective drug or medical device consultation. No fees unless we win.
How Do Defective Drug and Medical Device Cases Work?
Product liability law holds manufacturers, designers, distributors, and sellers responsible for harm caused by defective products. There are three main types of defect claims in drug and medical device cases:
- Design defects — the product’s design is inherently dangerous, meaning every unit made to that design poses a risk
- Manufacturing defects — an error during production caused a specific batch or unit to deviate from the intended design
- Failure to warn — the manufacturer knew of a risk but failed to adequately disclose it to patients or physicians
In many mass tort cases, all three theories apply. Drug and device manufacturers frequently learn of serious risks from clinical data, internal studies, or adverse event reports — and delay disclosure while continuing to sell. Cellino Law works with medical and scientific experts to establish what the manufacturer knew, when they knew it, and what they should have done differently.
Defective Medical Devices and Dangerous Drugs Cellino Law Handles
Cellino Law represents clients injured by a wide range of defective medical devices and dangerous drugs, including:
Hernia Mesh
Millions of hernia surgeries are performed each year using surgical mesh to reinforce weakened abdominal tissue. Defective polypropylene mesh products from manufacturers including Bard, Ethicon, Covidien, and Atrium have been linked to serious complications — chronic pain, infection, organ perforation, bowel obstruction, mesh migration, and hernia recurrence. Litigation is ongoing. A Bard hernia mesh settlement program has been established, Ethicon has settled thousands of cases, and Covidien bellwether trials are proceeding. New cases are still being accepted. Contact Cellino Law if you have experienced complications after hernia mesh surgery.
Hip Replacement Implants
Defective hip implants — particularly metal-on-metal designs — have caused metallosis (metal poisoning from microscopic particles released into surrounding tissue), implant loosening, device fracture, bone loss, and the need for painful revision surgeries. Major litigation against DePuy (more than $4 billion in settlements), Stryker ($1.4 billion in settlements), Zimmer Biomet, and others has resulted in significant recoveries for injured patients. Exactech is currently in bankruptcy proceedings. Cases involving recently discovered complications or less-common implant models continue to be filed. Contact Cellino Law to evaluate whether your implant is linked to active litigation.
Philips CPAP, BiPAP, and Ventilator Devices
Philips Respironics recalled millions of CPAP, BiPAP, and ventilator machines after polyester-based polyurethane foam used for sound abatement was found to degrade, releasing potentially toxic particles and gases that users could inhale or swallow. A $1.075 billion personal injury settlement was reached in 2024 and funded in early 2025; payments began distributing to eligible claimants in 2026. If you used a recalled Philips device and experienced cancer, respiratory illness, or other qualifying injuries, contact Cellino Law to evaluate your options.
Talcum Powder
Tens of thousands of women have filed lawsuits claiming that Johnson & Johnson’s talc-based baby powder and body powder products caused ovarian cancer and mesothelioma due to asbestos contamination. In July 2026, Johnson & Johnson proposed a $5.5 billion settlement to resolve approximately 76,000 ovarian cancer claims — the largest proposed resolution yet, though it is not yet final and requires approval from at least 95 percent of eligible claimants. Jury trials continue. If you or a loved one developed ovarian cancer or mesothelioma after long-term use of talcum powder products, contact Cellino Law about your eligibility.
Zantac (Ranitidine)
Zantac and generic ranitidine products were found to contain N-nitrosodimethylamine (NDMA), a probable human carcinogen, at levels that could increase cancer risk with prolonged use. The FDA recalled ranitidine products in 2020. GSK settled approximately 80,000 state-court Zantac claims for roughly $2.2 billion, with disbursements continuing through 2026. Cases against Boehringer Ingelheim, Pfizer, and Sanofi remain in active state-court litigation. If you took Zantac regularly and later developed cancer — particularly bladder, stomach, colorectal, pancreatic, or esophageal cancer — contact Cellino Law to evaluate your claim.
Bladder Sling (Pelvic Mesh)
Bladder slings and transvaginal pelvic mesh implants used to treat stress urinary incontinence and pelvic organ prolapse have caused serious complications in many patients, including chronic pain, infection, mesh erosion, organ damage, and worsening urinary problems. Multiple manufacturers settled pelvic mesh litigation for billions of dollars. If you experienced complications from a bladder sling or pelvic mesh implant, contact Cellino Law to evaluate your options.
Belviq (Lorcaserin)
The FDA recalled the weight-loss drug Belviq in 2020 after a clinical trial revealed a statistically significant increase in cancer risk — including pancreatic cancer, colorectal cancer, and lung cancer — among users compared to placebo. If you took Belviq and subsequently developed cancer, you may have a claim against the manufacturer. Contact Cellino Law for a free evaluation.
What Compensation Can Drug and Device Victims Recover?
- Medical expenses from treatment, revision surgeries, and rehabilitation
- Future medical costs for ongoing treatment
- Lost wages and reduced earning capacity
- Pain and suffering and emotional distress
- Wrongful death damages for surviving family members
Frequently Asked Questions
Do I need to know which specific device or drug harmed me to file a claim?
Not necessarily. Cellino Law can help you identify the manufacturer and model of your implant or the specific drug formulation you took through your medical records. If you experienced complications after a surgery, implant, or drug regimen, contact us and we will help evaluate whether you have a claim.
Is it too late to file?
Statutes of limitations for product liability claims vary by state — generally three years from the date of injury discovery in New York and two years in New Jersey and Connecticut. Many mass tort cases have specific filing deadlines tied to MDL enrollment or settlement programs. Contact Cellino Law immediately to ensure your claim is protected.
Does Cellino Law charge upfront fees?
No. Cellino Law handles all mass tort cases on a contingency fee basis. There are no upfront costs and no fees unless we win.
Contact Cellino Law About Your Defective Drug or Medical Device Case Today
If you or a loved one may have been harmed, contact Cellino Law for a free, no-obligation consultation. There are no upfront costs and no fees unless we win.
Call Cellino Law today at 888-888-8888 for a free defective drug or medical device consultation. No fees unless we win.
