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.

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-3038-2026

First seen by InfoSec Signals

Sep 23, 2026

Source: openFDA device recalls, U.S. Food and Drug Administration · about this source · more from it

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