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REFLECTION, MICROSTABLE 71740854Recalls & reported problems

Smith & Nephew, Inc. · REFLECTION LINER 28 INNER DIAMETER 54-56 OUTER DIAMETER 0 DEGREE SIZE F · Class 2

All models of REFLECTION, MICROSTABLE (16)

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 03596010231932), received between Sep 16, 2019 and Sep 16, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Material Integrity 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 18, 2026.

Most reported problems

Device problems

  • Material Integrity Problem1

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 16, 2019Material Integrity Problem; Material Integrity Problem

    IT WAS REPORTED THAT A REVISION SURGERY WAS PERFORMED DUE TO POLY WEAR. IMPLANT WAS ORIGINALLY PLACED IN 1996. LINER AND HEAD WERE REMOVED AND REPLACED.

    Patient problems: Injury

    MAUDE report 9068753 ↗

Other PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED devices

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Sources and updates

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