ATEC Lateral Navigation Disc Prep InstrumentsRecalls & reported problems across all models

We found 2 models of ATEC Lateral Navigation Disc Prep Instruments by Alphatec Spine, Inc. in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.

2 FDA recall records name at least one of these models by its device identifier, 2 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

ATEC Lateral Navigation Disc Prep Instruments recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

1. Jan 2, 2026Open, Classified

   Due a design issue where the navigated array connection geometry is incorrect.

   Z-1343-2026 · Root cause: Device Design · Recall details · FDA record ↗

2. Jan 2, 2026Open, Classified

   Due a design issue where the navigated array connection geometry is incorrect.

   Z-1342-2026 · Root cause: Device Design · Recall details · FDA record ↗

ATEC Lateral Navigation Disc Prep Instruments models

2 models, most reported first. Each model has its own page with its reports, recalls and device details.

• ATEC Lateral Navigation Disc Prep Instruments 266-01-000-10-N

  Orthopedic stereotaxic instrument
  1 recall0 reports
• ATEC Lateral Navigation Disc Prep Instruments 267-01-000-10-N

  Orthopedic stereotaxic instrument
  1 recall0 reports

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