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CHS 121107Recalls & reported problems

Smith & Nephew, Inc. · COMPRESSION HIP SCREW LAG SCREW 90MM 3.54IN · Class 2 · Implant

All models of CHS (30)

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 03596010061829), received between Sep 24, 2019 and Sep 24, 2019 — 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

  • Injury1

Recent adverse event reports

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

  • InjurySep 24, 2019Break; Break

    IT WAS REPORTED THAT A REVISION SURGERY WAS PERFORMED DUE TO A PATIENT FALL AND BROKEN IMPLANT.

    Patient problems: Injury

    MAUDE report 9112844 ↗

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Sources and updates

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