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FDA device recallVulnerabilitiesPublished Jun 11, 2026
Abbott Medical: Leadless Pacemaker
Updated under an hour ago ()
Software malfunction may occur during pacing capture threshold test of pacemaker resulting in programmer not successfully communicating the command to terminate the test.
- Tags
- FDA recall, medical device, class 3, Cardiovascular, Software Design Change, Open, Classified
- Related exam domains
- CISSP 3: Security Architecture and Engineering; CISSP 8: Software Development Security
- Source record id
- Z-2405-2026
- 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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