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LCP 226.661Recalls & reported problems

Synthes GmbH · 4.5MM BROAD LCP® PLATE 16 HOLES/296MM · 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 10886982159274), received between Sep 26, 2022 and Sep 26, 2022 — 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

  • Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjurySep 26, 2022Break; Break

    IT WAS REPORTED THAT THE PATIENT ORIGINALLY HAD SURGERY TO IMPLANT A 17-HOLE PLATE ON (B)(6) 2022. THEN, IT WAS REPORTED THAT ON (B)(6) 2022, THE PLATE WAS BROKEN. A REVISION SURGERY WAS PERFORMED ON (B)(6) 2022 USING A STRAIGHT BROAD PLATE TO REPLACE THE CURVED BROAD PLATE THAT WAS BROKEN. THIS REPORT INVOLVES ONE 4.5MM BROAD LCP® PLATE 16 HOLES/296MM. THIS IS REPORT 1 OF 1 FOR (B)(4).

    Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

    MAUDE report 15487665 ↗

Other PLATE, FIXATION, BONE devices

All PLATE, FIXATION, BONE devices →

Sources and updates

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