LCP 224.641Recalls & reported problems
Synthes GmbH · 4.5MM NARROW LCP® PLATE 14 HOLES/260MM · 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
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10886982158604), received between Mar 28, 2018 and Mar 28, 2018 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (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
- Break1
Patient problems
- Failure of Implant1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 28, 2018Break; Break
IT WAS REPORTED THAT THE PATIENT (PROFESSIONAL MOTORCYCLE DRIVER) HAD ORIGINAL SURGERY SOMETIME IN LATE 1986 FOR TREATMENT OF A FEMUR FRACTURE DUE TO A MOTOR VEHICLE ACCIDENT (MVA). PATIENT WAS IMPLANTED WITH AN UNKNOWN SYNTHES NAIL AND AN UNKNOWN QUANTITY AND TYPE OF SCREWS. ON AN UNKNOWN DATE POST-OPERATIVELY, PATIENT HAD HEALED WELL AND THE NAIL CONSTRUCT WAS REMOVED WITH NO FURTHER ISSUES. ON (B)(6) 2014, PATIENT WAS STRUCK BY A MOTOR VEHICLE, RESULTING IN A FRACTURED FEMUR, TIBIA, AND FIBULA. THESE INJURIES REQUIRED MORE THAN NINETEEN (19) SURGERIES. ON (B)(6) 2014, THE FEMUR AND TIBIA FRACTURES WERE PLATED. IT IS REPORTED THAT ONE OF THE PLATES WAS THE 4.5MM VARIABLE ANGLE LOCKING COMPRESSION PLATE (VA-LCP) CURVED CONDYLAR PLATE 16 HOLE 336MM-RIGHT. NO ISSUE WAS REPORTED. ON AN UNKNOWN DATE BETWEEN 2016 AND 2017, WHILE RIDING HIS MOTORCYCLE PATIENT WAS AGAIN INVOLVED IN A MOTOR VEHICLE ACCIDENT. THE PATIENT¿S FEMUR WAS AGAIN BROKEN. THE TWO (2) PLATES WERE ALSO BROKEN. ON UNKNOWN DATE, PATIENT WAS RETURNED TO SURGERY WHERE THE BROKEN PLATES AND SCREWS WERE REMOVED. PATIENT WAS REVISED TO A 95-DEGREE BLADE PLATE AND SCREWS TO ADDRESS THE NEW FEMUR FRACTURE. PATIENT IS CURRENTL
Patient problems: Failure of Implant
MAUDE report 7378186 ↗
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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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