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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.
Open the source record- 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.