LCP 422.256Recalls & reported problems
Synthes GmbH · TI LCP(TM) DISTAL FEMUR PLATE 11 HOLES/276MM-RIGHT · 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 10886982215444), received between Jul 21, 2021 and Jul 21, 2021 — classified as 1 injury.
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 16, 2026.
Most reported problems
Device problems
- Device-Device Incompatibility1
- Migration1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJul 21, 2021Device-Device Incompatibility; Migration; Device-Device Incompatibility; Migration
IT WAS REPORTED THAT DURING A PROCEDURE ON AN UNKNOWN DATE, THE SCREWS EITHER BACKED OUT OR WERE BROKEN. THE PATIENT WAS REVISED WITH ANOTHER PLATE. PROCEDURE WAS WITH AN UNKNOWN DELAY. PATIENT OUTCOME IS UNKNOWN. THIS REPORT IS FOR A TITANIUM (TI) LOCKING COMPRESSION PLATE (LCP) DISTAL FEMUR PLATE. THIS IS REPORT 1 OF 2 FOR (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions; Pain
MAUDE report 12205073 ↗
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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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