Showing 41 results for "Defective Medical Devices"
Weitz & Luxenberg associate attorney EricaRae Garcia has written “Get Prepped for DMEs,” appearing in the May 2022 issue of Trial. The magazine is published by the American Association for Justice (AAJ). In her article, Ms. Garcia offers guidance on the complexity of addressing defense medical examinations (DMEs). These exams are sometimes given the misnomer…
UPDATE 3/8/2024: Read the most current information about this litigation. Philips announced a voluntary recall of some of its sleep and respiratory care devices in mid-June. The U.S. Food and Drug Administration (FDA) announced the recall was issued for multiple devices, based on the risk of injury. The FDA has not classified this recall. However, on…
The Department of Justice of the United States has settled for $9.1 million with manufacturer 3M Company to recover damages for allegedly defective combat earplugs that 3M sold to the U.S. military for over a decade, without any admission of liability by 3M. The lawsuit and settlement allege 3M knew the earplugs were defective even…
Weitz & Luxenberg feels privileged to spread the news: Ellen Relkin received the American Association for Justice (AAJ) Lifetime Achievement Award. As many of us know, there is no one more deserving of this important award, highlighting Ms. Relkin’s achievements throughout her career. As a W&L partner and chair of the firm’s Drug and Medical…
Weitz & Luxenberg is accepting cases for investigation from clients who developed TASS after undergoing cataract surgery and receiving Bausch + Lomb recalled lenses. This recall involves specific models of intraocular lenses. Bausch + Lomb issued a voluntary recall of its enVista Aspire™, enVista Envy™, and certain enVista® Monofocal intraocular lenses (IOL) on April 3,…
Weitz & Luxenberg is accepting clients suffering due to the failure of the Zimmer Biomet CPT Hip System. Many people now face revision surgery after a defective hip replacement. Recent research indicates a risk of post-surgical thigh bone fracture above that of other similarly designed hip systems. Zimmer Biomet issued a voluntary recall of its…
Weitz & Luxenberg is accepting cases from clients who suffered burns after they, or a loved one, underwent an electrosurgical procedure using Megadyne Mega 2000 or Mega Soft Patient Return Electrodes. Megadyne’s “patient return electrodes are used during monopolar electrosurgery.” These devices are used during surgeries. If you were badly burnt and injured by this…
Weitz & Luxenberg is currently accepting legal cases from clients who became seriously ill, or had a loved one die, after using an Amplatzer Steerable Delivery Sheath cardiac catheter. This medical device is used in heart procedures and was manufactured by Abbott. Abbott recalled its Amplatzer Steerable Delivery Sheath (ASDS) due to a recognized increased…
Weitz & Luxenberg is pleased to announce our women partners — Lisa Nathanson Busch, Robin Greenwald, and Ellen Relkin — are presenting at multiple legal events this winter. They are sharing their knowledge and experience at several professional events. Among their goals are connecting with colleagues who are also striving to achieve the best outcomes for clients….
Weitz & Luxenberg attorney, EricaRae Garcia, served as a panelist on a Mass Torts Made Perfect Webinar on the Chemical Hair Relaxer Litigation. The event was held virtually. Ms. Garcia is a key member of W&L’s Drug and Medical Device Litigation unit. Since her arrival, Ms. Garcia has been passionate about seeking justice for clients…