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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

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.

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