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29 posts tagged with “Medical Devices”
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Although federal law requires the reporting of adverse events, no reports concerning power morcellators had been received by the U.S. Food and Drug Administration (FDA) prior to December 2013, according to The Cancer Letter. Prior to December 2013, the FDA had received no Medical Device…
A medical study published in the October 2015 issue of the Annals of Surgery takes a closer look at whether trauma patients actually benefit from having inferior vena cava (IVC) filters implanted, or instead face a greater risk of life-threatening complications associated with the filters…
IVC filters are inserted through an artery and deployed with spider-like legs designed to both catch blood clots before they find their way to the lung and cause what could potentially be a fatal pulmonary embolism, and to hold the filter in place at the…
A new complaint filed by Mr. and Mrs. Duffie of Georgia joins more than two dozen Bard G2 IVC filter lawsuits that have been centralized for pretrial proceedings before Arizona U.S. District Judge David G. Campbell. Atlanta injury law firm Childers, Schlueter & Smith LLC,…
The U.S. Food and Drug Administration (FDA) recently revised its May 2015 warning to now include an increased risk of bone fractures and decreased bone mineral density. Bone mineral density relates to the strength of a person’s bones. The original FDA warning stated that SGLT2…
The IVC (inferior vena cava) filter is a spider-like medical device used to filter blood clots and prevent them from reaching a patient’s lungs and causing a pulmonary embolism, which could mean permanent lung damage or even death. Despite the advantages of IVC filters, they…
Based on the recent updates and a study concerning Invokana* for type II diabetes, there seem to be a lot of questions being asked about its use and whether it is the best option for a particular patient. Although these questions are best presented to…
Transvaginal mesh devices are surgically implanted in women to treat pelvic organ prolapse (POP) and stress urinary incontinence (SUI). The devices are designed to prevent internal organs from coming into contact with each other, but have resulted in numerous complications for patients, including: M
The U.S. Food and Drug Administration is unleashing a barrage of quality-control initiatives aimed at overseas drug manufacturing, potentially empowering prosecutors who choose to target those companies with sloppy production techniques. The campaign played a large part in FDA Commissioner Margaret
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