Each year thousands of unsuspecting people are injured by defective drugs and/or medical devices. In order to prevent these defective products from reaching the public, certain protocols and regulations have been established and placed on the manufacturers by the FDA. When a company fails to properly investigate their product and/or fails to report any problems or side effects, they put the public’s health in jeopardy. Injuries sustained from using defective prescription drugs or medical devices can not only cause tremendous pain but also financial hardship.
Our team has extensive experience in identifying and vigorously pursuing claims for all of our clients who have been affected by defective pharmaceutical drugs or medical device products.
Top-selling prescription drug Abilify may be associated with compulsive gambling
Popular rheumatoid arthritis drug, Actemra, may be causing a mass of complications such as heart attacks and heart failure
FDA announced it requested Allergan to remove certain textured surface implants
We represent patients alleging that Caremark and CVS Health failed to provide proper shipping procedures
DePuy ASR hip replacement system recalled after reports indicate a high failure rate
Some patients reported complications such as device loosening and an increased need for early revision surgery
Women are reporting that the permanent birth control device is causing severe and painful injuries
Some ranitidine medicines contain a substance that may cause cancer.
Hepatitis C Outbreak has caused serious concerns prompting a class action
Patients have experienced the severe complications and issues with their metal-on-metal hips
The FDA issued a black-box warning following reports that patients experienced injuries resulting from sleep behaviors.
Black-box warning for the popular type-2 diabetes drug Invokana
Invokana, a popular type 2 diabetes drug, has been linked to serious side effects, including kidney cancer.
Patients are reporting serious injuries including perforation or other damage to organs
The FDA issued a Safety Communication about a potentially serious problem involving Medtronic pacemakers.
Women implanted report that the IUDs break during removal surgery
Cardiovascular risks associated with Onglyza or Kombiglyze
Certain St. Jude defibrillators may experience premature battery depletion
Stryker hip replacements are linked to a high early failure rate, resulting in early revision surgery
New reports have surfaced regarding problems with the Stryker LFIT V40 component
A number of Tritanium cups have come loose causing pain and other complications
Women using talcum powder and later developing ovarian cancer
Thousands of women may have been unnecessarily exposed to a significant risk of injuries
Viagra may be putting certain men at risk for developing a dangerous form of skin cancer
Some birth defects and health risks in newborns have been linked to Zofran
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