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FDA device recallVulnerabilitiesPublished June 11, 2026

Abbott Medical: Leadless Pacemaker

Software malfunction may occur during pacing capture threshold test of pacemaker resulting in programmer not successfully communicating the command to terminate the test.

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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
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.