Defective Medical Devices

Mass tort litigation has been pending against the manufacturers of NuvaRing for many years now and is hopefully drawing to a close in the coming months.  The litigation is primarily based in federal court in St. Louis, Missouri, where MDL No. 1964 has been pending since 2008.  The MDL is […]

Lawyers preparing for trial in product liability cases, such as Searcy Denney, can never comment on settlement talks – but that has not stopped Bloomberg News from speculating that Johnson & Johnson may be close to offering more than $3 billion to settle its recalled him implant cases in the U.S. […]

We will never know just how much Wanda Queen was offered by C.R. Bard to settle her defective Bard Avaulta Solo transvaginal mesh lawsuit. All we do know is that on the morning that opening arguments were set to be heard, August 21, in the Charleston, West Virginia federal court, […]

Cook Medical is once again shipping the Zilver PTX Drug-Eluting Peripheral Stent to doctors and hospitals in Europe, Japan and in the U.S. following a global recall due to at least one fatality. The stent was voluntarily recalled after the company received 13 complaints of a faulty delivery system. Specifically, […]

The national litigation efforts in state and federal court involving Wright Medical’s defective metal-on-metal hip implant products ( Conserve®,Dynasty®, Profemur® and the Lineage®) have been proceeding well over the past few months with additional progress expected through the end of 2013.  The coordinated litigation efforts in both the federal Multi-District Litigation (MDL) […]

The entire trial took just 11 days. Donna Cisson sued C.R. Bard Co. of New Jersey, maker of the Avaulta Plus transvaginal mesh implanted in her in 2009 to treat pelvic organ prolapse. Last week, the jury awarded the 55-year-old Cisson $250,000 in compensatory damages and $1.75 million in punitive […]

With more than 27,000 transvaginal mesh cases consolidated in one federal court in West Virginia, the first bellwether case is now in its second week. Donna Cisson, 55 was implanted with a Bard Avaulta Plus Posterior BioSynthetic Support System in May 2009. She has undergone several removal operations after pain […]

Hurry up and wait appears to be the word from the U.S. Food and Drug Administration (FDA) when it comes to the safety of medical devices. The agency was supposed to have issued a final proposal by the end of June on a mandate to make it easier to identify […]

Saying this was the first mistrial he had declared in his 20 years on the bench, U.S. District Judge Joseph R. Goodwin ended a product liability trial naming C.R. Bard after a witness for the plaintiffs made a statement that could not be undone. Dr. Lennox Hoyte, a female pelvic […]

The first federal transvaginal mesh trial that names manufacturer C.R. Bard begins this week in Charleston, West Virginia. Plaintiff Donna Cisson was implanted with the Bard Avaulta Plus Posterior on May 8, 2009 in Toccoa, Georgia. Bard Urological, a division of C.R. Bard, Inc. designed, labeled, manufactured and sold the […]