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VA-LCP 02.111.690SRecalls & reported problems

Synthes GmbH · 2.4/2.7 VA-LCP 2-C DRP STD 6H HD/13H SHAFT/186MM/RT-STER · Class 2 · Implant

All models of VA-LCP (256)

Data updated Oct 18, 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 10886982032195), received between Oct 20, 2022 and Oct 20, 2022 — 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 18, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Unspecified Tissue Injury1

Recent adverse event reports

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

  • InjuryOct 20, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT ON AN UNKNOWN DATE, THERE WAS INTRA-ARTICULAR FRACTURE FIXATION FOR DISTAL RADIUS WITH EXTENSION TO RADIAL DIAPHYSIS. POSTOPERATIVE COMPLICATION WAS EXTENSIVE BONE LOSS FROM TRAUMA REQUIRED BONE GRAFTING AT A LATER DATE. THIS REPORT IS FOR ONE (1) 2.4/2.7 VA-LCP 2-C DRP STD 6H HD/13H SHAFT/186MM/RT-STER THIS IS REPORT 1 OF 12 FOR COMPLAINT (B)(4).

    Patient problems: Unspecified Tissue Injury

    MAUDE report 15642396 ↗

Other Plate, fixation, bone devices

All Plate, fixation, bone devices →

Sources and updates

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