FDA: Software Failure Behind 24% of Last Year's Medical Device Recalls

In response, FDA told Threatpost that it is developing tools to disassemble and test medical device software and locate security problems and weak design

Do we, the patients, have the right to do this, or does it have to go on behind closed doors and NDAs?

In a distopian novel, the government would do this so that they could turn off your heart, if you said anything out of turn.

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