Recall
Active
FDA
Official source
Alphatec Spine, Inc.: SafeOp Patient Interface, REF: AIX11240, part of SafeOp 3: Neural Informatix System Recall
Intraoperative neuromonitoring device, due to a software issue, may experience loss or interruption of triggered electromyography (tEMG) functionality during use, displaying as system...
- Company
- Alphatec Spine, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration