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LCP 222.662SRecalls & reported problems

Synthes GmbH · 4.5MM LCP® CONDYLAR PLATE 12 HOLES/278MM/RIGHT-STERILE · 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 10886982157416), received between May 15, 2018 and May 15, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Break” (1 report).

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 15, 2018Break; Break

    IT WAS REPORTED THAT ON AN UNKNOWN DATE, THE SHAFT OF THE PATIENT'S IMPLANTED VARIABLE ANGLE (VA)-LOCKING COMPRESSION PLATE (LCP) CONDYLAR PLATE SNAPPED. THE PATIENT THEN UNDERWENT HARDWARE REVISION SURGERY ON (B)(6) 2018, WHERE THE BROKEN PLATE WAS REMOVED EASILY AND REPLACED. THERE WAS NO PATIENT INFORMATION REPORTED. IT IS UNKNOWN IF THERE WAS SURGICAL DELAY AND WHAT THE PATIENT OUTCOME WAS. NO ADDITIONAL INFORMATION AVAILABLE. THIS IS REPORT 1 OF 1 FOR (B)(4).

    Patient problems: Failure of Implant

    MAUDE report 7515769 ↗

Other PLATE, FIXATION, BONE devices

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Sources and updates

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