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FDA device recallVulnerabilitiesPublished September 11, 2026
Philips North America: Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Due to software malfunction, patient information system may freeze and become unresponsive.
Open the source record- 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
- 9/23/2026
Exam domain labels come from a keyword heuristic and are study hints, not an official mapping. The summary is the publisher's own text, shortened; the linked record is authoritative.