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PRECICE Plating SystemRecalls & reported problems across all models

Nuvasive Specialized Orthopedics, Inc. · 67 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 Plating System model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.

Adverse event reports
24
Deaths reported
0
Injuries reported
13
Recalls
3

We found 67 models of PRECICE Plating System by Nuvasive Specialized Orthopedics, Inc. in the FDA's device registry (GUDID). Together they are named in 24 adverse event reports in the FDA's MAUDE database, received between Feb 22, 2021 and Nov 30, 2021 — classified as 13 injuries, 11 malfunctions.

The most frequently reported specific device problem is “Corroded” (13 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 Plating 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 64 of these models · Recall details · FDA record ↗

  2. Feb 12, 2021Open, Classified

    Due to complaints of adverse events potentially related to biological safety. The complaints included report of pain and bony abnormalities at the interface between the telescoping nail segments.

    Z-1325-2021 · Root cause: Under Investigation by firm · names 65 of these models · Recall details · FDA record ↗

  3. Feb 12, 2021Open, Classified

    Due to complaints of adverse events potentially related to biological safety. The complaints included report of pain and bony abnormalities at the interface between the telescoping nail segments.

    Z-1323-2021 · Root cause: Under Investigation by firm · names 65 of these models · Recall details · FDA record ↗

Most reported PRECICE Plating System problems

Device problems

  • Corroded13
  • Adverse Event Without Identified Device or Use Problem9
  • Material Twisted/Bent4
  • Material Discolored3
  • Unstable1

Patient problems

  • No Clinical Signs, Symptoms or Conditions6
  • Deformity/ Disfigurement4
  • Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available3
  • Insufficient Information3
  • Failure of Implant2
  • Impaired Healing2
  • Osteolysis2
  • Wound Dehiscence2

PRECICE Plating System models

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

Recent PRECICE Plating System adverse event reports

The 15 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