LCP 02.108.421Recalls & reported problems
Synthes GmbH · PEDIATRIC LCP CONDYLAR PLATE 5.0MM/90°/5 HOLES · 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 10886982030115), received between Jul 20, 2018 and Jul 20, 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
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJul 20, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT UNDERWENT REVISION SURGERY ON (B)(6) 2018 DUE TO FIBROUS DYSPLASIA WHICH EVENTUALLY LED TO HIP FALLING INTO EXTREME VARUS. PATIENT PREVIOUSLY HAD AN OSTEOTOMY, ON AN UNKNOWN DATE, AND WAS IMPLANTED WITH A PEDIATRIC LOCKING COMPRESSION PLATE (LCP) CONDYLAR PLATE, FOUR (4) UNKNOWN LOCKING SCREWS AND FOUR (4) UNKNOWN CORTEX SCREWS. DURING THE REVISION, THE PLATES AND SCREWS WERE TAKEN OUT SUCCESSFULLY AND SECTION OF THE FIBROUS DYSPLASIA WAS TAKEN OUT. THE PATIENT'S NEW OSTEOTOMY WAS THEN CORRECTED WITH A CUSTOM RETROGRADE NAIL. THE PROCEDURE WAS COMPLETED SUCCESSFULLY. IT IS UNKNOWN IF THERE WAS A SURGICAL DELAY. PATIENT OUTCOME REPORTED AS GOOD. THIS REPORT IS FOR ONE (1) PEDIATRIC LCP CONDYLAR PLATE 5.0 MM/90°/5 HOLES. THIS IS REPORT 1 OF 3 FOR (B)(4).
Patient problems: No Code Available
MAUDE report 7706348 ↗
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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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