Skip to content

PROFEMUR® PHAPCLE3Recalls & reported problems

Microport Orthopedics Inc. · PROFEMUR® PLASMA Z CLASSIC SIZE 3 VARUS 8 DG SHORT NECK · Class 2 · Implant

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 M684PHAPCLE31), received between Aug 4, 2021 and Aug 4, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Migration” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Migration1

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.

  • InjuryAug 4, 2021Migration; Migration

    ALLEGEDLY, THERE WAS A STEM SUBSIDENCE. ADDITIONAL INFORMATION RECEIVED ON 07/15/2021 FROM SALES REP (B)(4): PRODUCT ID'S AND LOT NUMBERS OF COMPONENTS INVOLVED, IMPLANTATION AND REVISION FACILITIES' NAME, DATE OF ORIGINAL SURGERY, DATE OF REVISION.

    Patient problems: Insufficient Information

    MAUDE report 12278713 ↗

Other Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented devices

All Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.