Topic: FDA safety alert

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.

The FDA disclosed over 60 safety reports related to intra-aortic balloon pumps manufactured by Maquet and Datascope, following a recall this summer.

GE Healthcare recalled two of its infant warmers due to side panels and latches that may crack, break or open, allowing infants to fall.

The FDA warned diabetes patients of the risks of using homegrown treatment devices, such as unrecognized combos of CGMs and insulin pumps.

The FDA said it has not yet established the long-term benefits and risks of robotic surgery for cancer, compared to traditional open surgery.