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Precice CTL4.5-044-SRecalls & reported problems

Nuvasive Specialized Orthopedics, Inc. · 4.5mm x 44mm Screw, Locking, PL · Class 2 · Implant

All models of Precice (38)

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

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887517029850), received between May 26, 2021 and May 26, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

  • Break1

Patient problems

  • Insufficient Information1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMay 26, 2021Break; Break

    INFORMATION WAS RECEIVED THAT DURING REMOVAL, THE LOCKING SCREW BROKE. IT IS BELIEVED THAT THE SCREW BROKE DUE TO EXCESSIVE TORQUE APPLIED FROM THE POWER DRILL.

    Patient problems: Insufficient Information

    MAUDE report 11887051 ↗

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Sources and updates

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