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FDA device recallVulnerabilitiesPublished June 3, 2026
GE Medical Systems China Co., Ltd.: Transmitters And Receivers, Electrocardiograph, Telephone
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.
Open the source record- 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
- 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.