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The Baxter LIfe2000 device, with the software version noted in the advisory, is also part of an FDA recall (https://www.fda.gov/medical-devices/ventilator-correction-baxter-healthcare-updates-use-instructions-life2000-ventilation-system-due)

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Thanks for the heads up. Unfortunately, I stopped routinely checking FDA action on vulnerabilities reported by CISA because their actions have been so far and few between. It is almost like they do not care about vulnerable medical devices.

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