LEVEL ONE THORACIC, STERILE 24-015-29-71Recalls & reported problems
KLS-Martin L.P. · PLATE, RIB, LOCKING, X SHP, 2.3 MM SCREW, 15 MM BAR, 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
- 6
- Deaths reported
- 0
- Injuries reported
- 6
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00888118121288), received between Jan 2, 2020 and Aug 8, 2025 — classified as 6 injuries.
The most frequently reported specific device problem is “Break” (4 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
- Break4
- Fracture2
Patient problems
- Impaired Healing4
- Discomfort2
- Insufficient Information1
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
InjuryAug 8, 2025Fracture; Fracture
IT WAS REPORTED A PLATE FRACTURED. IT WAS REMOVED.
Patient problems: Insufficient Information
MAUDE report 22754829 ↗InjuryOct 27, 2022Fracture; Fracture
TWELVE MONTHS AFTER IMPLANT PATIENT PRESENTED WITH NEW COMPLAINT OF DISCOMFORT AND RIB PLATE ON A HEALED RIB WAS FOUND TO BE FRACTURED ON A RADIOGRAPH. THE PHYSICIAN ELECTED TO REMOVE THE PLATE PER THE FACILITY'S "STANDARD PROCEDURE." NO ADDITIONAL HARDWARE WAS IMPLANTED ON THE HEALED RIB. CAUSE OF PLATE FRACTURE AFTER CONSOLIDATION UNKNOWN.
Patient problems: Discomfort
MAUDE report 15685937 ↗InjuryFeb 11, 2021Break; Break
IT WAS REPORTED A PREVIOUSLY BROKEN PLATE AND WAS REMOVED.
Patient problems: Impaired Healing
MAUDE report 11317925 ↗InjuryDec 10, 2020Break; Break
IT WAS REPORTED THAT A PLATE BROKE AND IS EXPECTED TO BE REMOVED ON AN UNKNOWN DATE.
Patient problems: Impaired Healing
MAUDE report 10983741 ↗InjuryDec 4, 2020Break; Break
IT WAS REPORTED A PLATE BROKE AND WAS REMOVED.
Patient problems: Discomfort; Impaired Healing
MAUDE report 10943343 ↗InjuryJan 2, 2020Break; Break
IT WAS REPORTED A PLATE BROKE. THE PLATE WILL NOT BE REMOVED.
Patient problems: Impaired Healing
MAUDE report 9537643 ↗
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- PRECICE® Plating System LP4.5-MLT4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls5 reports
- 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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