LCP 426.662Recalls & reported problems
Synthes GmbH · 4.5MM TI CURVED BROAD LCP® PLATE 16 HOLES/300MM · 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 10886982217363), received between May 19, 2023 and May 19, 2023 — 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, K092609); 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
- 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.
InjuryMay 19, 2023Break; Break
DEVICE REPORT FROM SYNTHES REPORTS AN EVENT IN GERMANY AS FOLLOWS: LEGAL CASE: IT WAS REPORTED FROM INBOX ON (B)(6) 2023 THAT A LETTER WAS RECEIVED FROM A LAW FIRM IN MUNICH. IT IS ABOUT ALLEGED PRODUCT LIABILITY DAMAGE. THE PATIENT WAS HOSPITALIZED ON (B)(6) 2022 IN THE ABOVE. A TITANIUM PLATE IS INSTALLED IN THE HOSPITAL FOR THE SUPPLY OF A FEMORAL NECK BOOK. THE METAL PLATE GOT BROKEN ON (B)(6) 2022 WITHOUT ANY RECOGNIZABLE INFLUENCE OF FORCE OR OTHER RECOGNIZABLE CAUSE. THE PATIENT SUSPECTS A MATERIAL DEFECT. THERE WAS A REVISION O. THE PATIENT SUFFERS FROM MULTIPLE SCLEROSIS. THIS REPORT IS FOR ONE (1) 4.5MM TI CURVED BROAD LCP® PLATE 16 HOLE THIS IS REPORT 1 OF 1 FOR COMPLAINT (B)(4).
Patient problems: Failure of Implant
MAUDE report 16961800 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K000682, K041911, K092609. 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.
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- PRECICE® Plating System LP4.5-MLT4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls5 reports
- PRECICE® Plating System LP4.5-PLF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- PRECICE® Plating System LP4.5-MRT4BNuvasive 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-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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