Back to signals
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.