LCP 02.114.007Recalls & reported problems
Synthes GmbH · 1.5MM LCP T-PLATE/4H HEAD 8 HOLE SHAFT · Class 2 · Implant
All models of LCP (367)
Data updated Oct 18, 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 10886982034847), received between Mar 12, 2025 and Mar 12, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device-Device Incompatibility” (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
- Device-Device Incompatibility1
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.
MalfunctionMar 12, 2025Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT PATIENT UNDERWENT OPEN REDUCTION AND FIXATION OF A PHALANX IN A HAND FRACTURE ON (B)(6) 2025. THE GUIDE DID NOT THREAD EASILY INTO THE BLOCKED HOLES. IT HAD BEEN DECIDED TO USE A 1.5 PLATE. THE DOCTOR WAS INFORMED IN ADVANCE THAT THE LCP EQUIPMENT HAD BEEN SENT TO HIM. THE PLATE WAS TRIMMED AND IMPLANTED. THE LOCKING GUIDE DID NOT THREAD INTO THE HEAD HOLES, SO THE DOCTOR DECIDED TO DRILL FREEHAND. THE SCREWS DID NOT LOCK, CAUSING INSTABILITY OF THE FRACTURE. THE DOCTOR DECIDED TO REMOVE THE HARDWARE AND LEAVE PINS FROM THE INSTITUTION. THE SPECIALIST PREFERABLY REQUIRED HAND-HELD EQUIPMENT.
Patient problems: Insufficient Information
MAUDE report 21587505 ↗
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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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