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VA-LCP 04.117.704Recalls & reported problems

Synthes GmbH · 2.7MM/3.5MM TI VA-LCP EXT MEDL DHP 4H/LT/111MM-LONG · 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 10886982106803), received between Feb 23, 2021 and Feb 23, 2021 — classified as 1 injury.

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

1 other recall cover devices cleared under the same FDA submission (K120070); they may or may not involve this specific model.

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

  • 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.

  • InjuryFeb 23, 2021Break; Break

    IT WAS REPORTED THAT ON (B)(6) 2021, THE PATIENT UNDERWENT A HARDWARE REMOVAL OF BROKEN SYNTHES PLATES AND SCREWS. THERE WERE EIGHT (8) 2.7MM BROKEN SCREWS AND TWO (2) 3.5MM BROKEN SCREWS. HARDWARE WAS SUCCESSFULLY REMOVED. PATIENT OUTCOME IS UNKNOWN. NO FURTHER INFORMATION PROVIDED. CONCOMITANT DEVICES REPORTED: 3.5MM TI LCP HOOK PLATE 3 HOLE (PART# 04.113.103, LOT # UNKNOWN, QUANTITY 1), 3.5MM TI LCP® POSTEROLATERAL DISTAL HUMERUS PLATE 5H-LEFT (PART# 441.265, LOT # UNKNOWN, QUANTITY 1), 2.7MM SCREW (PART# UNKNOWN, LOT # UNKNOWN, QUANTITY 8), 3.5MM SCREW (PART# UNKNOWN, LOT # UNKNOWN, QUANTITY 2). THIS REPORT IS FOR ONE (1) 2.7MM/3.5MM TI VA-LCP EXT MEDL DHP 4H/LT/111MM-LONG. THIS IS REPORT 2 OF 10 FOR (B)(4). THIS COMPLAINT INVOLVES TOTAL 13 DEVICES. THIS (B)(4) REPORTS TOTAL 10 DEVICES WHILE REMAINING 3 DEVICES ARE REPORTED UNDER RELATED (B)(4).

    Patient problems: Failure of Implant

    MAUDE report 11366793 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K120070. One submission often covers many models, so check the product and lot details in each record.

  • Z-0124-2016 · Sep 28, 2015 · Terminated
    Synthes 2.7MM/3.5MM VA-LCP Medial Distal Humerus Plates 10H/RT/186mm- Sterile and Synthes 2.7MM/3.5MM VA-LCP Extended Medial Distal Humerus Plates 10H/RT/189mm-Sterile The Synthes

Other PLATE, FIXATION, BONE devices

All PLATE, FIXATION, BONE devices →

Sources and updates

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