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PRECICE Trauma Nail SystemRecalls & reported problems across all models

Nuvasive Specialized Orthopedics, Inc. · 182 models in the FDA device registry

Data updated Oct 16, 2026 from official FDA records · Editorial policy

3 open recalls name at least one PRECICE Trauma Nail System model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.

Adverse event reports
4
Deaths reported
0
Injuries reported
2
Recalls
3

We found 182 models of PRECICE Trauma Nail System by Nuvasive Specialized Orthopedics, Inc. in the FDA's device registry (GUDID). Together they are named in 4 adverse event reports in the FDA's MAUDE database, received between Sep 6, 2019 and Feb 23, 2021 — classified as 2 injuries, 2 malfunctions.

The most frequently reported specific device problem is “Defective Device” (2 reports).

3 FDA recall records name at least one of these models by its device identifier, 3 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

PRECICE Trauma Nail System 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. Oct 29, 2021Open, Classified

    The Instructions for Use have been updated to include: (1) Clarification that the device is intended for use only in patients 18 years and older, (2) That patients should weigh 50 lbs. or more while undergoing treatment, and (3) That no more than two devices should be implanted at a time.

    Z-0319-2022 · Root cause: Device Design · names 182 of these models · Recall details · FDA record ↗

  2. Feb 12, 2021Open, Classified

    Due to not having the full complement of biological assessments for all potential patients and as a result the devices are not indicated for use in individuals under the age of 18 years old.

    Z-1350-2021 · Root cause: Device Design · names 182 of these models · Recall details · FDA record ↗

  3. Feb 12, 2021Open, Classified

    Due to not having the full complement of biological assessments for all potential patients and as a result the devices are not indicated for use in individuals under the age of 18 years old.

    Z-1349-2021 · Root cause: Device Design · names 127 of these models · Recall details · FDA record ↗

Most reported PRECICE Trauma Nail System problems

Device problems

  • Defective Device2
  • Adverse Event Without Identified Device or Use Problem1
  • Mechanical Problem1

Patient problems

  • Failure of Implant3
  • Nerve Damage1

PRECICE Trauma Nail System models

182 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.

Recent PRECICE Trauma Nail System adverse event reports

The 4 most recent reports across all models, in the reporter's own words as published by the FDA.

Other Nuvasive Specialized Orthopedics, Inc. products

All Nuvasive Specialized Orthopedics, Inc. devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page