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Alphatec Spine, Inc.

Alphatec Spine, Inc.: 2 recalls listed since February 2026 across FDA.

By year

  • 20262

By agency

  • FDA2

By category

  • Medical Device2

All recalls (2)

SafeOp Patient Interface

The device may experience loss or interruption of triggered electromyography functionality during use.

Moderate risk, FDA, , Software defect

ATEC Lateral Navigation Disc Prep Instruments

ATEC Lateral Navigation Disc Prep Instruments have a design issue with incorrect navigated array connection geometry.

Moderate risk, FDA, , Device defect
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