LEVEL ONE THORACIC, STERILE 24-015-27-71Recalls & reported problems
KLS-Martin L.P. · PLATE, RIB, LOCKING, LONG Y, 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
- 7
- Deaths reported
- 0
- Injuries reported
- 7
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 00888118101419), received between Apr 28, 2017 and Jul 21, 2025 — classified as 7 injuries.
The most frequently reported specific device problem is “Break” (3 reports).
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
- Break3
- Fracture3
- Insufficient Device Problem Information1
- Osseointegration Problem1
Patient problems
- Impaired Healing2
- Insufficient Information2
- Device Embedded In Tissue or Plaque1
- Inadequate Osseointegration1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
InjuryJul 21, 2025Fracture; Fracture
IT WAS REPORTED FOLLOWING APPROXIMATELY FIFTEEN MONTHS OF IMPLANTATION A THORACIC PLATE BECAME FRACTURED POSSIBLY DUE TO PATIENT CONDITION. A PORTION OF IT WAS REMOVED AND REPLACED.
Patient problems: Insufficient Information
MAUDE report 22555407 ↗InjuryApr 27, 2023Insufficient Device Problem Information; Insufficient Device Problem Information
A Y-SHAPED PLATE BROKE AT OR AFTER IMPLANT AND WAS SUBSEQUENTLY REPLACED.
Patient problems: Insufficient Information
MAUDE report 16824397 ↗InjuryDec 29, 2021Break; Break
THE PHYSICIAN REPORTED THAT A RIB PLATE BROKE DUE TO PATIENT NON-COMPLIANCE. THE PLATE WAS REMOVED AND REPLACED.
Patient problems: Impaired Healing
MAUDE report 13109800 ↗InjuryNov 24, 2020Break; Break
IT WAS REPORTED A PLATE BROKE. THE PLATE IS NOT EXPECTED TO BE REMOVED AT THIS TIME.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 10898979 ↗InjuryFeb 15, 2019Break; Break
IT WAS REPORTED PLATES BROKE AND WERE REMOVED.
Patient problems: Impaired Healing
MAUDE report 8344772 ↗InjuryJun 1, 2017Fracture; Osseointegration Problem; Fracture; Osseointegration Problem
PLATE FRACTURED AFTER IT WAS IMPLANTED IN THE PATIENT. THE PATIENT CAN FEEL THE PLATE MOVE WHEN MOVING AND IS IN PAIN. THE PLATE IS BEING LEFT IN THE PATIENT FOR NOW. IF PAIN DOES NOT DECREASE OVER TIME, THE PLATE WILL BE REMOVED.
Patient problems: Inadequate Osseointegration
MAUDE report 6606125 ↗InjuryApr 28, 2017Fracture
THREE RIB PLATES FRACTURED THAT WERE PREVIOUSLY IMPLANTED. REMOVAL OF THE PLATES WILL BE SCHEDULED FOR (B)(6) 2017.
Patient problems: Device Embedded In Tissue or Plaque
MAUDE report 6531005 ↗
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- PRECICE® Plating System LP4.5-MRT4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- 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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