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FDA device recallVulnerabilitiesPublished Sep 11, 2026
Philips North America: Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Updated 5 hours ago ()
Due to software malfunction, patient information system may freeze and become unresponsive.
- Tags
- FDA recall, medical device, class 2, Cardiovascular, Software design, Open, Classified
- Related exam domains
- CISSP 3: Security Architecture and Engineering; CISSP 8: Software Development Security
- Source record id
- Z-3142-2026
- First seen by InfoSec Signals
- Sep 23, 2026
Source: openFDA device recalls, U.S. Food and Drug Administration about this source more from it
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