LCP 242.121Recalls & reported problems
Synthes GmbH · 4.5MM LCP® PROXIMAL FEMUR HOOK PLATE 4 HOLES/169MM · Class 2 · Implant
All models of LCP (367)
Data updated Oct 16, 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 10886982168085), received between Sep 7, 2022 and Sep 7, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Deformation” (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 16, 2026.
Most reported problems
Device problems
- Material Deformation1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 7, 2022Material Deformation; Material Deformation
IT WAS REPORTED THAT ON AN UNKNOWN DATE, DURING POST OP INSPECTION OF GRAPHIC CASES IT WAS NOTED THAT THERE WAS WHITE RESIDUE ON UNIVERSAL SMALL FRAG GRAPHIC CASES. NUMBERS ARE WORN OFF ON SCREW RACK, AND LONG NITINOL SHAFTS HAVE BENT TIPS X 3. PROXIMAL FEMUR PLATE WAS BENT DURING STERILIZATION. THERE WAS NO PATIENT INVOLVEMENT THEREFORE NO PATIENT CONSEQUENCES. THIS REPORT INVOLVES ONE 4.5MM LCP® PROXIMAL FEMUR HOOK PLATE 4 HOLES/169MM. THIS IS REPORT 2 OF 4 FOR (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15370721 ↗
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- PRECICE® Plating System LP4.5-DRF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls1 report
- PRECICE® Plating System LP4.5-PLF40Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 reports
- PRECICE® Plating System LP4.5-PRT42Nuvasive 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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