LCP 02.124.204Recalls & reported problems
Synthes GmbH · 3.5MM LCP PROXIMAL TIBIA PLATE LOW BEND 6 HOLES/102MM/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 10886982042491), received between Jul 17, 2018 and Jul 17, 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
- Discomfort1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJul 17, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT ON (B)(6) 2018, PATIENT UNDERWENT REMOVAL OF ONE (1) LOCKING COMPRESSION (LCP) PROXIMAL TIBIA PLATE, UNKNOWN NUMBER OF CORTEX SCREWS AND LOCKING SCREWS OF THE RIGHT KNEE DUE TO DISCOMFORT. THE HARDWARE WAS ORIGINALLY IMPLANTED ON FEBRUARY 2017. ALL DEVICES WERE SUCCESSFULLY REMOVED. IT IS UNKNOWN IF THERE WAS A SURGICAL DELAY. PATIENT OUTCOME IS UNKNOWN. THIS IS REPORT 1 OF 3 FOR (B)(4).
Patient problems: Discomfort
MAUDE report 7695026 ↗
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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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