Drugs & Medical Device Defect Attorneys
Each year, defective and dangerous drugs and medical devices cause thousands of injuries and deaths in the United States. Often, pharmaceutical manufacturing giants recall their products from the market long after they have become aware of their potential for injury. As a result, thousands of people each year suffer personal and catastrophic injury, undergo multiple corrective surgeries, and even lose their lives.
At Robinson Calcagnie, Inc., we understand the devastating effects dangerous drugs and defective medical devices can have on the lives of our clients and their families. As a nationally recognized leader in the representation of victims of dangerous drugs and defective medical devices, we have over 30 years experience representing clients who have suffered life-changing injuries, damages and losses as a result of unsafe products.
For more information regarding drug recalls and dangerous medical devices, contact the California defective drug injury lawyers at (888) 348-8855 today. Our Newport Beach office location represents people throughout Orange County, San Diego County, Los Angeles County, Riverside County, and San Bernardino County, and in conjunction with local counsel licensed in other jurisdictions throughout the United States.
Dangerous Drugs and Defective Medical Devices
Robinson Calcagnie, Inc. currently represents clients in cases involving a number of prescription drugs and medical devices, including:
Drugs
- Invokana® & Other SGLT2 Inhibitors
- Risperdal®
- Testosterone Therapy
Dangerous Medical Devices
- DePuy ASR & Pinnacle Hip Implants
- Morcellator Lawsuits
- Transvaginal Mesh & Vaginal Sling Implants
- Caldera Transvaginal Mesh
When Manufacturers Knowingly Put the Public at Risk
Too often, in their efforts to rush new drugs onto the market, manufacturers ignore safe practices and fail to conduct adequate testing that could have revealed the dangers of their products. In certain cases, drug manufacturers and medical device makers are aware of dangers associated with their products before ever placing them on the market. Approval of a product by the FDA does not immunize the manufacturer from liability, and deaths and injuries can occur even when the drugs have been used according to the manufacturers’ warnings and instructions.
Some are the result of defective warnings and labels, which fail to adequately warn of drug interactions, adverse reactions and serious side effects; fail to provide instructions for safe use; or do not provide information regarding contraindications or preexisting conditions which increases the risk of injury. Others are caused by drugs that are recalled or withdrawn from the market, which were never safe to begin with, and which would not have been approved but for the manufacturer misleading or withholding material data from the FDA. Click here to read an amicus brief summarizing numerous cases of fraudulent conduct by pharmaceutical companies.
Demanding Answers and Compensation
Robinson Calcagnie, Inc. has the resources and experience required to take on drug manufacturing giants. Our defective drug and medical device lawyers obtain and assemble the necessary evidence and retain teams of top-flight medical and scientific experts and consultants to hold pharmaceutical companies and medical device makers accountable.
Contact Robinson Calcagnie, Inc. Today to Schedule a Free Consultation
If you or a loved one has been seriously injured as a result of a defective product, dangerous drug or faulty medical device and would like your case evaluated, contact the California lawyers at Robinson Calcagnie, Inc. today. We provide free consultations and are available to meet with you even if you are unable to travel.