Defective drugs, medical devices and household products injure thousands of Americans every year. Many assume that if a product is on the market, it’s undergone rigorous testing by the government, but that’s not always the case.
As we noted in an article a few weeks ago, efforts by the Food and Drug Administration to make it easier for companies to introduce new products may be jeopardizing patient safety; demands to cut through the red tape of regulatory review have led to consumers being exposed to pricey drugs of dubious efficacy, with potentially serious (or simply unknown) side effects, as well as implanted medical devices with a high rate of defects or failure.
When the regulatory process fails to protect the public, courts of law offer possible relief to those harmed by that lapse. Some recent product liability lawsuits have been attracting considerable comment, both because of the sheer scope of the often-complex litigation and the staggering jury verdicts or hard-fought settlements they have produced. Among those that have attracted headlines in recent months:
THE PRODUCT LIABILITY LAWYERS AT FDAZAR
If you have suffered injuries from a dangerous drug or the failure of a defective medical device, you may be entitled to compensation. The product liability attorneys at Franklin D. Azar & Associates can help answer your questions concerning several devices associated with recalls, adverse events, or possibly inadequate warnings issued to doctors and patients, including talcum powder injuries, Attune Knee Systems, St. Jude Defibrillators, and the blood thinners Xarelto, Eliquis and Pradaxa. Contact us for a free, no-obligation consultation.