The corrective action is the software fix (it's already out as 2.7.1). It's the preventative action that would be interesting, but we probably won't see that.

The corrective action is the software fix (it's already out as 2.7.1). It's the preventative action that would be interesting, but we probably won't see that. The specific recall action in the FDA database is here: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=206914 https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res... It simply says "Software Design Change" as FDA determined root cause... so super vague. EDIT: Although the root cause might be software, it's possible that they did detect the crashing during testing, but did not characterize it fully, and/or missed a step in their risk assessment analysis to determine that it may impact battery life and therefore have risk of harm to life.