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 […]
Category: Defective Medical Devices
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 […]
Many of our clients who have hip prosthesis wonder if they should have an image taken even though they are not experiencing any pain. A new study suggests that may not be a bad idea. Published in the May issue of The Journal of Bone and Joint Surgery, researchers find […]
Unlike other countries, the United States has no way to monitor medical devices after they are approved and used or implanted in patients. It is sort of the Wild West out there. When a medical device is defective and injures a patient, the patient, her doctor or lawyer have the […]
It is still uncertain why and how many American Medical Systems (AMS) transvaginal mesh victims are affected, but Endo Health Solutions Inc, which bought the company, has agreed to settle a small number of AMS cases. Endo has agreed to pay $54.5 million to settle product liability or defective product […]
Consumers may not realize it, but the U.S. Food and Drug Administration (FDA) currently has no way to track problems with medical devices and drugs that go wrong other than voluntary reporting. Unlike other countries that have drug and device registries, the FDA has an absolute head-in-the sand approach to […]
The Food and Drug Administration (FDA) held a meeting this week to consider whether the 510(k) approval process for medical devices is keeping the public safe while balancing the need of industry to get innovative products to the market faster and easier. “External stakeholders” were invited and helped set the […]
The Biomet MDL (multidistrict litigation) was established for the organization and litigation of individual personal injury lawsuits against Biomet in the fall of 2012. In February of this year, the MDL contained 132 individual lawsuits. The count now stands upwards of 180 individual lawsuits, and it is still growing every […]
