LCP 422.253Recalls & reported problems
Synthes GmbH · TI LCP(TM) DISTAL FEMUR PLATE 7 HOLES/196MM-LEFT · 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 10886982215383), received between May 27, 2018 and May 27, 2018 — classified as 1 injury.
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
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- No Code Available1
- Nonunion/Delayed-union Bone Fracture1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 27, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT UNDERWENT HARDWARE REMOVAL AND REVISION OF A DISTAL FEMORAL SHAFT ON (B)(6) 2018 DUE TO NON-UNION. THE REMOVED HARDWARE INCLUDED A 7-HOLE LESS INVASIVE STABILIZATION SYSTEM (LISS) PLATE AND SEVEN (7) LOCKING SCREWS. LISS PLATE WAS REMOVED SO THAT A NEW PLATE CAN BE PLACED ON THE LATERAL SIDE FOR THE REVISION. THE ORIGINAL IMPLANT DATE IS UNKNOWN. ALL THE DEVICES WERE REMOVED INTACT. THE PROCEDURE WAS COMPLETED SUCCESSFULLY. THERE WAS NO SURGICAL DELAY. PATIENT OUTCOME IS UNKNOWN. THIS REPORT IS FOR ONE (1) TI LCP(TM) DISTAL FEMUR PLATE 7 HOLES/196MM-LEFT. THIS IS REPORT 1 OF 2 FOR (B)(4).
Patient problems: No Code Available; Nonunion/Delayed-union Bone Fracture
MAUDE report 7547214 ↗
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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
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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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