Alphatec Spine recalls

Recall found. Alphatec Spine is named in FDA Class II recall Z-2793-2026 covering SafeOp Patient Interface. Hazard: 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. Identifying details: UDI-DI: 00190376517506. System Set ID/Patient Interface Serial Number: 2007716/ DG106225, 2005498/ DG106220, 2005490/ DG106230. Status: Ongoing.

Models with recalls

SafeOp Patient Interface (1)

All Alphatec Spine recalls

FDA Class II · Medical device · July 29, 2026

SafeOp Patient Interface recall — Alphatec Spine, Inc.

Intraoperative neuromonitoring device, due to a software issue, may experience loss or interruption of triggered electromyography (tEMG) functionality during use, displaying as sys…

Official ID Z-2793-2026 · Official record ↗

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Compiled from official public-domain government data. Last checked September 7, 2026 at 6:00 AM UTC.