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Profemur PPW38023Recalls & reported problems

Microport Orthopedics Inc. · PROFEMUR 175MM STEM BOWED/TAPER SIZE 13 · Class 3 · Implant

All models of PROFEMUR (116)

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 M684PPW380231), received between Sep 3, 2021 and Sep 3, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Loss of Osseointegration” (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

  • Loss of Osseointegration1

Patient problems

  • Insufficient Information1

Recent adverse event reports

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

  • InjurySep 3, 2021Loss of Osseointegration; Loss of Osseointegration

    ALLEGEDLY, A PATIENT WAS REVISED FOR STEM LOOSENING. COMPONENTS NOT REVISED: UNKNOWN SHELL, UNKNOWN PART ID.

    Patient problems: Insufficient Information

    MAUDE report 12422495 ↗

Other Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented devices

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Sources and updates

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