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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

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.

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