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A boxed warning is the strongest type of caution against the potential hazards a product could pose to consumers. Often called a black box warning, it is something the Food and Drug Administration (FDA) recommends for medications and medical devices … LEARN MORE
Allergan BIOCELL® textured breast implants and tissue expanders have been recalled worldwide due to an uncommon incidence of Breast Implant-Associated Anaplastic Large Cell Lymphoma (BIA-ALCL), a rare cancer of the immune system. On July 25, 2019, the U.S. Food and Drug … LEARN MORE
JULY 13, 2015 UPDATE: NBC NEWS BROADCAST IN DEPTH LOOK AT TAKATA RECALL AND DEATH OF JEWEL BRANGMAN. JUNE 19, 2015 UPDATE: HONDA CONFIRMS THE DEATH OF JEWEL BRANGMAN CAUSED BY DEFECTIVE TAKATA AIR BAG. READ THE LATEST DETAILS HERE. Panish … LEARN MORE
Important Information About the CRE Infection Litigation from the Medical Device Legal Experts at Panish Shea & Boyle LLP Nearly 200 patients at Ronald Reagan UCLA Medical Center, more than 70 patients at Cedars-Sinai Medical Center in Los Angeles and … LEARN MORE
On February 23, 2015, Panish Shea & Boyle LLP filed the first CRE superbug lawsuit against Olympus America, Inc., Olympus Corporation of the Americas, and Olympus Medical System Corporation (collectively, “Olympus”) relating to the CRE “superbug” infection that was spread among Ronald … LEARN MORE
A couple weeks ago, the Food and Drug Administration announced its intention to revisit testosterone supplement therapy. This was due to recent research that called into question whether or not the users of such products could be susceptible to heightened … LEARN MORE
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