VentStar and ID Breathing Circuits and Anesthesia Sets have been recalled because some of the devices may not have been correctly assembled, which may have resulted in a short circuited breathing hose.
Sales of electronic cigarettes could be halted if companies do not stop marketing the devices to youth.
Due to the federal government shutdown, the US Food and Drug Administration has only about 5 weeks of funding left to review new drug applications.
The pea-sized device is a self-expanding wire mesh that is inserted through an incision in the leg and guided through vessels to the heart, where it is placed to seal the opening.
The consequence of the shutdown means the budget appropriated by Congress for the Agency is on hold, resulting in approximately 7000 of it’s 17,000 employees being furloughed.
In animal studies, the treatment was associated with improvement in both motor and cognitive function.
The FDA announcement came a day after the release of findings from an investigation into medical device safety worldwide.
While approved in Europe, Asia and Latin America, tianeptine is an unscheduled pharmaceutical agent in the US that has been linked to serious adverse events, including death, when used for recreational purposes.
The approval was based on data from a single-arm, open-label sequential cohort study in which patients received Promacta in combination with horse antithymocyte globulin (h-ATG) and cyclosporine.
Aemcolo is a broad spectrum, semi-synthetic, orally-administered, minimally-absorbed antibiotic designed to allow for delayed release to the colon.
