We have previously reported on the ongoing cybersecurity issues with St. Jude defibrillators [view related posts here, here, and here]. On June 29, 2018, the Food and Drug Administration (FDA) classified the required firmware updates to St. Jude defibrillators as Class 2 recalls, which is the medium-severity category of classifications that is applicable to issues where adverse health consequences are considered temporary or reversible.
Please see full publication below for more information.
