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FDA device recallVulnerabilitiesPublished Jan 22, 2026
Philips North America: Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Updated 3 hours ago ()
A recent software (SW) patch modifies Mobile Event Notification filter settings without providing any indication to the user when upgrading the system.
- Tags
- FDA recall, medical device, class 2, Cardiovascular, Software Design Change, Open, Classified
- Related exam domains
- CISSP 3: Security Architecture and Engineering; CISSP 7: Security Operations; CISSP 8: Software Development Security; CISM 4: Incident Management
- Source record id
- Z-1156-2026
- 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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