Three people, including a train engineer, were injured on Wednesday when a Long Island Rail Road train hit a livery cab on the tracks west of Wyandanch station, LIRR officials said.
LIRR spokesman Salvatore Arena said the driver of the Lincoln Town Car was taken to Good Samaritan Hospital Medical Center ...
Parker Waichman LLP, a national law firm, just filed a lawsuit on behalf of a Colorado woman allegedly injured by transvaginal mesh products manufactured by American Medical Systems, Inc. The suit was filed on May 21, 2012 in the U.S. District Court for the Northern District of California (Case No. ...
In light of a recent outbreak linked to contaminated duodenoscopes, the U.S. Food and Drug Administration (FDA) is questioning manufacturers about their methods for cleaning the devices, the New York Times reports. The specialized scopes, which have been linked to several outbreaks in recent years, most recently infected seven patients ...
A national law firm is not satisfied with the way the U.S. Food & Drug Administration (FDA) has handled warnings regarding Actos (pioglitazone) bladder cancer risks. In a statement published today, Parker Waichman LLP called on the FDA to compel Takeda Pharmaceuticals, the maker of the type 2 diabetes drug, ...
Early results from the largest study to date to compare Pradaxa and warfarin indicate that in a real-world setting, Pradaxa causes more complications than decades-old warfarin. The preliminary study results were announced last week, during the 2012 Thrombosis and Hemostasis Summit of North America.
Medical device giant, Medtronic Inc., is settling charges over kickbacks to doctors. The firms just agreed to pay $23.5 million to settle claims it paid physicians kickbacks in exchange for their use of its pacemakers and defibrillators, according to a U.S. Justice Department announcement yesterday.
The company was accused of seeking ...
According to a new study, failing metal-on-metal hip implants generate toxic nano-particles that release Cobalt 2+ ions, which not only cause inflammation in surrounding tissue, but have the potential to cause long-term damage to the genetic material of cells. According to a report published by Medicalxpress.com, this “genotoxicity” could ...
Victims of alleged Pradaxa injuries are awaiting word on whether their lawsuits will be consolidated in a multidistrict litigation. According to a report from The Madison Record, so far just over two dozen Pradaxa bleeding lawsuits have been filed in federal courts throughout the U.S.
A warning at the end of May 2016 was issued by Intuitive Surgical concerning a risk that small particles could be introduced inside the heart during intra-cardiac procedures using its da Vinci Xi device. The da Vinci Xi received U.S. … Continue reading →
A new study has revealed that, based on insurance claim information, bladder cancer patients may not benefit from robotic surgery for their bladder removal procedures. In fact, according to Fierce Medical Device, patients experienced similar complication rates and hospital stay … Continue reading →
A recent motion to remand was granted in a Medtronic InFuse case. The case will be returned back to its Circuit Court to continue with trial. InFuse is a genetically engineered, synthetic, recombinant human Bone Morphogenetic Protein (rhBMP-2). The product … Continue reading →
Intuitive Surgical, which manufactures and markets the da Vinci surgical robot, just released information concerning quarterly sales, which have declined by almost half, and that the drop is related, in part, to thousands of lawsuits brought over alleged da Vinci … Continue reading →
A recent print ad for the da Vinci surgical robot system, which is manufactured and marketed by Intuitive Surgical, has created significant controversy and opened questions about a possible conflict of interest. The University of Illinois allowed its name and … Continue reading →
A recent report reveals that adverse reactions associated with da Vinci surgical robot procedures may be greater than believed. The under-reporting of actual patient injuries may be presenting a different picture of the surgical technology to prospective surgical patients. The … Continue reading →
Two recent actions involving more than 110,000 components of Intuitive Surgical’s da Vinci surgical robot system have been deemed Class II recalls by the U.S. Food and Drug Administration (FDA). The FDA’s Class II designation involves situations in which “use … Continue reading →
In its second warning this month, Intuitive Surgical Inc., the manufacturer of the da Vinci robot surgery system, advised physicians that friction in the arms of some devices might cause unit stalls. The Urgent Medical Device Recall notice was issued … Continue reading →
Mounting reports of adverse events during robotic surgeries have led to increased government scrutiny and a cautionary statement issued by the American College of Obstetricians and Gynecologists. “Robotic surgery is not the only or the best minimally invasive approach to … Continue reading →
The controversy surrounding risks tied to robotic surgery systems, specifically with the da Vinci robot, are being seen in the United Kingdom. The da Vinci was cleared for use in 2000 in the United States by the U.S. Food and … Continue reading →