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FDA device recallVulnerabilitiesPublished Jun 3, 2026
GE Medical Systems China Co., Ltd.: Transmitters And Receivers, Electrocardiograph, Telephone
Updated 2 hours ago ()
Software in development inadvertently made available for customer use. Use of this software version can result in clinical information being associated with the incorrect patient. This could impact clinical decision-making.
- Tags
- FDA recall, medical device, class 2, Cardiovascular, Software Manufacturing/Software Deployment, Open, Classified
- Related exam domains
- CISSP 3: Security Architecture and Engineering; CISSP 8: Software Development Security
- Source record id
- Z-2306-2026
- 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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