Medical device failures brought to light now bolster lawsuits by Christina Jewett, Kaiser Health News Tuesday, December 3, 2019 A vast cache of FDA records released this summer, covering tens of thousands of device safety reports, have begun taking on a life of their own.
FDA discloses patient deaths linked to recalled balloon pumps by Conor Hale Wednesday, November 20, 2019 The FDA disclosed over 60 safety reports related to intra-aortic balloon pumps manufactured by Maquet and Datascope, following a recall this summer.
GE recalls infant bed warmers due to cracking side panels by Conor Hale Monday, July 15, 2019 GE Healthcare recalled two of its infant warmers due to side panels and latches that may crack, break or open, allowing infants to fall.
FDA warns against DIY insulin systems, citing overdose by Conor Hale Monday, May 20, 2019 The FDA warned diabetes patients of the risks of using homegrown treatment devices, such as unrecognized combos of CGMs and insulin pumps.
FDA warns public against unapproved robotic cancer surgeries by Conor Hale Friday, March 1, 2019 The FDA said it has not yet established the long-term benefits and risks of robotic surgery for cancer, compared to traditional open surgery.