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EVOS 72465405Recalls & reported problems

Smith & Nephew, Inc. · EVOS 2.7MM/3.5MM POSTEROLATERAL DISTAL FIBULA PLATE 5 HOLE RIGHT 93MM · Class 2 · Implant

All models of EVOS (190)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00885556648612), received between Jul 3, 2020 and Jul 3, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Connection Problem” (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

  • Connection Problem1

Patient problems

  • No Information1

Recent adverse event reports

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

  • MalfunctionJul 3, 2020Connection Problem; Connection Problem

    PLATE PART NO: 72465405 (NOT FOUND ON SEARCH BY NUMBER OR DESCRIPTION). IT WAS REPORTED THAT DURING SURGERY THE SURGEON WAS UNABLE TO GET LOCKING SCREW HEADS TO ENGAGE WITH TABS IN HOLE OF PLATE. IT IS UNKNOWN IF THERE WAS A DELAY. THERE IS NO INJURY REPORTED AND A S&N BACK UP DEVICE WAS AVAILABLE TO FINISH THE SURGERY.

    Patient problems: No Information

    MAUDE report 10228603 ↗

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Sources and updates

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