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FDA device recallVulnerabilitiesPublished July 23, 2026

Alphatec Spine, Inc.: Stimulator, Electrical, Evoked Response

Intraoperative neuromonitoring device, due to a software issue, may experience loss or interruption of triggered electromyography (tEMG) functionality during use, displaying as system faults, loss of communication between the Patient Interface and Tablet, and prompts requiring system reboot; may result in increased operative time and surgical plan change.

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Tags
FDA recall, medical device, class 2, Neurology, Software Design Change, Open, Classified
Related exam domains
CISSP 3: Security Architecture and Engineering; CISSP 7: Security Operations; CISSP 8: Software Development Security; CISM 4: Incident Management
Source record id
Z-2793-2026
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.