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PROFEMUR® PLSSS011Recalls & reported problems

Microport Orthopedics Inc. · PROFEMUR® RENAISSANCE® CLASSIC STD FLARE SZ 11 STR 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 M684PLSSS0111), received between Dec 24, 2019 and Dec 24, 2019 — 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

  • No Information1

Recent adverse event reports

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

  • InjuryDec 24, 2019Migration; Migration

    ALLEGEDLY, IT APPEARS THAT THE STEM HAS SUBSIDED. STEM WAS WELL FIXED AND A LONGER HEAD WAS USED WITH A SLEEVE FROM MICROPORT (28MM DELTA OPTION HEAD AND XL SLEEVE). LEFT HIP.

    Patient problems: No Information

    MAUDE report 9515895 ↗

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.