LCP 226.642Recalls & reported problems
Synthes GmbH · 4.5MM CURVED BROAD LCP® PLATE 14 HOLES/265MM · 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 10886982159229), received between Mar 23, 2021 and Mar 23, 2021 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (1 report).
1 other recall cover devices cleared under the same FDA submission (K000682, K041911, K082807); they may or may not involve this specific model.
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
- Unspecified Tissue Injury1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 23, 2021Break; Break
IT WAS REPORTED THAT ON (B)(6) 2021, THE PATIENT UNDERWENT REVISION DUE TO CURVE BROAD LOCKING COMPRESSION PLATE BREAKAGE AT THE ISTHMUS. INITIALLY, PATIENT HAD A ZIMMER TOTAL DISTAL FEMORAL REPLACEMENT ON (B)(6) 2021 AND HAD A LOCKING COMPRESSION PLATE (LCP) CURVED CROAD PLATE PLACED TO HELP SUPPORT THE JUNCTION BETWEEN CUT AND PROXIMAL FEMUR FOR ADDITIONAL SUPPORT. THE PATIENT WAS CONVERTED TO A FULL STEM DISTAL FEMORAL PROSTHESIS. THE SURGEON MENTIONED THAT THE PATIENT HAD GREAT CORTEX AT SURGERY AND WAS SUPPOSED TO BE NON-WEIGHT BEARING FOR 6 WEEKS. PATIENT SAYS HE DID NOT WALK ON IT. PLATE WAS REMOVED SAFELY AND THE PATIENT WAS THEN CONVERTED TO A FULL DISTAL FEMORAL REPLACEMENT. IT IS UNKNOWN IF THERE WAS SURGICAL DELAY. PROCEDURE OUTCOME IS UNKNOWN. NO PATIENT CONSEQUENCE. THIS REPORT IS FOR ONE (1) 4.5 CURVED BROAD LCP PL 14 HOLES/265. THIS IS REPORT 1 OF 1 FOR (B)(4).
Patient problems: Unspecified Tissue Injury
MAUDE report 11556155 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K000682, K041911, K082807. One submission often covers many models, so check the product and lot details in each record.
- Z-0409-2014 · Jul 30, 2013 · TerminatedSynthes 4.5 mm LCP Curved Condylar Plate Intended for buttressing multifragmentary distal femur fractures.
Other APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT devices
- PRECICE® Plating System LP4.5-DLF31Nuvasive Specialized Orthopedics, Inc. · Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component3 recalls0 reports
- R3 71364451Smith & Nephew, Inc. · APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT145 reports
- DFS HA BONE SCREWS HAA60-11030Biomet Orthopedics, LLC · APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT2 recalls0 reports
- DFS HA BONE SCREWS HAA60-15040Biomet Orthopedics, LLC · APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT2 recalls0 reports
- DFS HA BONE SCREWS HAB60-12040Biomet Orthopedics, LLC · APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT2 recalls0 reports
- DFS HA BONE SCREWS HAA60-18040Biomet Orthopedics, LLC · APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT2 recalls0 reports
- DFS HA BONE SCREWS HAA60-15060Biomet Orthopedics, LLC · APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT2 recalls0 reports
- DFS HA BONE SCREWS HAA60-15020Biomet Orthopedics, LLC · APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT2 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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