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

