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FDA device recallVulnerabilitiesPublished August 27, 2026

GE Medical Systems Information Technologies Inc: Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

Software issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults following the update and will not follow the alarm settings previously configured for each patient or care area.

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Tags
FDA recall, medical device, class 2, Cardiovascular, Device Design, Open, Classified
Related exam domains
CISSP 3: Security Architecture and Engineering; CISSP 7: Security Operations; CISSP 8: Software Development Security
Source record id
Z-3039-2026
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.