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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.
Open the source record- 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.