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Profemur PPW38005Recalls & reported problems

Microport Orthopedics Inc. · PROFEMUR 135MM STEM STRAIGHT/TAPER SIZE 15 · 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 M684PPW380051), received between Sep 6, 2021 and Sep 6, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Fracture” (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

  • Fracture1

Patient problems

  • Bone Fracture(s)1

Recent adverse event reports

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

  • InjurySep 6, 2021Fracture

    ALLEGEDLY, A PATIENT WAS REVISED FOR GREATER TROCHANTER FRACTURE. COMPONENTS NOT REVISED: PRODUCT NAME: PROFEMUR(R) PROXIMAL BODY PART ID: PPW39104. PRODUCT NAME: PROFEMUR(R) ROUGHENED DISTAL STEM, TAPERED PART ID: PPW38005. PRODUCT NAME: UNKNOWN CUP, UNKNOWN PART ID AND LOT NUMBER.

    Patient problems: Bone Fracture(s)

    MAUDE report 12430952 ↗

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

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Sources and updates

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