LEVEL ONE THORACIC, STERILE 24-015-36-71Recalls & reported problems
KLS-Martin L.P. · PLATE, RIB, LOCKING, X SHP, SOLID, RIGID, 2.3 MM SCREW, CP TITANIUM · Class 2 · Implant
All models of LEVEL ONE THORACIC, STERILE (30)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00888118128881), received between Feb 2, 2022 and Jun 4, 2025 — classified as 2 injuries.
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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
- Fracture1
Patient problems
- Discomfort1
- Impaired Healing1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJun 4, 2025Fracture; Fracture
IT WAS REPORTED FOLLOWING APPROXIMATELY ONE YEAR OF IMPLANTATION THE THORACIC PLATES BECAME FRACTURED LIKELY DUE TO INITIAL IMPROPER TECHNIQUE. THEY WERE REMOVED AND REPLACED.
Patient problems: Discomfort
MAUDE report 22143791 ↗InjuryFeb 2, 2022Break; Break
IT WAS REPORTED THAT A PLATE BROKE DUE TO NON-COMPLIANCE, AND A PRE-EXISTING CONDITION. IT WAS REMOVED.
Patient problems: Impaired Healing
MAUDE report 13426871 ↗
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- PRECICE® Plating System LP4.5-PLF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- PRECICE® Plating System LP4.5-DRF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls1 report
- PRECICE® Plating System LP4.5-MLT42Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 reports
- PRECICE® Plating System LP4.5-MRT42Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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