LEVEL ONE CMF 25-314-85-91Recalls & reported problems
KLS-Martin L.P. · PLATE, MICRO, L SHP, 100*, LEFT, 1.5 MM SCREW, CP TITANIUM · Class 2 · Implant
All models of LEVEL ONE CMF (150)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00888118038722), received between Oct 5, 2018 and May 20, 2021 — classified as 4 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 16, 2026.
Most reported problems
Device problems
- Break3
- Adverse Event Without Identified Device or Use Problem1
- Use of Device Problem1
Patient problems
- Impaired Healing3
- Scar Tissue1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryMay 20, 2021Break; Adverse Event Without Identified Device or Use Problem; Break; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT A PLATE BROKE DUE TO PATIENT GRINDING THEIR TEETH AND WAS REMOVED.
Patient problems: Impaired Healing
MAUDE report 11854613 ↗InjuryAug 19, 2020Break; Break
IT WAS REPORTED A PLATE BROKE AND WAS REMOVED.
Patient problems: Impaired Healing
MAUDE report 10427507 ↗InjuryAug 1, 2019Break; Break
IT WAS REPORTED THAT THE PLATES BROKE. THEY WERE REMOVED AND REPLACED.
Patient problems: Impaired Healing
MAUDE report 8850517 ↗InjuryOct 5, 2018Use of Device Problem; Use of Device Problem
IT WAS REPORTED THE PLATES WERE SITTING PROUD. THE PLATES WERE REMOVED.
Patient problems: Scar Tissue
MAUDE report 7939736 ↗
Other PLATE, BONE devices
- MatrixNEURO 04.503.104.01Synthes GmbH · PLATE, BONE252 reports
- RapidSorb 806.004.02SSynthes GmbH · PLATE, BONE146 reports
- TruMatch SD980.001Materialise NV · Plate, Bone1 recall21 reports
- Matrix 04.511.225.01Synthes GmbH · PLATE, BONE62 reports
- NA 400.834Synthes GmbH · PLATE, BONE58 reports
- TruMatch SD980.016Materialise NV · Plate, Bone55 reports
- ProPlan CMF SD900.101Materialise NV · Plate, Bone1 recall1 report
- TruMatch SD980.013Materialise NV · Plate, Bone1 recall0 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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