Archive for 2019
Updates on the September 11th Victim Compensation Fund Extension Legislation
House of Representatives Votes in Favor of VCF Extension On Friday, July 12th, 2019, the U.S. House of Representatives voted by a large margin to reauthorize the September 11th Victim Compensation Fund until the year 2090. The September 11th Victim Compensation Fund (VCF) provides compensation to those whose health has been impacted by 9/11 and…
Read MoreSPBMC Member Eleni Coffinas Obtains $1.5 Million Settlement for Disabled Client in Medical Malpractice Case
SPBMC Member Eleni Coffinas recently obtained a $1.5 million settlement for a previously disabled client who suffered further disabling injuries after a fall in a nursing home facility. Ms. Coffinas’ client, a 34-year-old man who had a pre-existing severe brain injury due to a prior brain hemorrhage, was admitted into a rehabilitation facility in February…
Read MoreSPBMC Proudly Sponsors 22nd Annual Thurgood Marshall Junior Mock Trial Competition
SPBMC Managing Member Thomas J. McManus, Member Vito A. Cannavo and Associate Steve V. Fils-Aime recently attended the 22nd Annual Thurgood Marshall Junior Mock Trial Program Closing Ceremony. SPBMC is the main sponsor of the program, which was established in 1997 by Judge Elizabeth A. Taylor to enrich and empower the lives of middle school…
Read MoreHouse Judiciary Committee Unanimously Votes in Favor of VCF Extension After Testimony from SPBMC Client and Jon Stewart, Among Others
After powerful testimony from several key figures, including SPBMC client and retired FDNY Lieutenant Michael O’Connell and former Daily Show host and 9/11 victims advocate Jon Stewart, the House Judiciary Committee unanimously voted in favor of an extension to the Victim Compensation Fund (VCF). The VCF will be extended through 2090. Also present at the…
Read MoreVast Archive of Defective Medical Devices To Be Opened
Since 1999, the Food and Drug Administration (FDA) has implemented an Alternative Summary Reporting program for medical device manufacturers. Under this program, medical device makers had the authority to report incidents of patient injuries, illnesses, and even deaths due to device malfunctions only to the FDA and not to the public. The Alternative Summary Reporting…
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