A device out of service support since 2014 was still running in enough hospitals to warrant a recall in 2025. That is the legacy-device problem stated plainly.

GE HealthCare recalled legacy MUSE cardiology information systems after determining an outside party could access them to view and manipulate stored patient data. Around 4,200 systems, with the oldest, Muse 5, unsupported since 2014. No CVE, this came through the FDA recall path, and the remediation is upgrade or replace plus hardening: strong passwords, staff awareness, all the compensating controls a hospital applies because the product itself can no longer be fixed.

End of support has to mean something a customer can act on. Communicate it early, clearly, with a migration path, or you get a decade-old system holding cardiac records with no patches coming.