PROFEMUR® PHA0CLS5Recalls & reported problems
Microport Orthopedics Inc. · PROFEMUR® Z CLASSIC STEM SZ 5 STRAIGHT SHORT NECK · Class 2 · Implant
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI M684PHA0CLS51), received between Feb 5, 2025 and Feb 6, 2025 — classified as 2 injuries.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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.
Reports received per month
Most reported problems
Device problems
- Device Dislodged or Dislocated1
- Insufficient Device Problem Information1
Patient problems
- Insufficient Information1
- Pain1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryFeb 6, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
INFORMATION FROM CLINICAL STUDY # (B)(4): PATIENT #65 REPORTED THE FOLLOWING ADVERSE EVENTS: PAIN. THIS ADVERSE EVENT DID NOT END UP IN REVISION SURGERY.
Patient problems: Pain
MAUDE report 21324498 ↗InjuryFeb 5, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated
ALLEGEDLY, PATIENT UNDERWENT THR ON (B)(6) 2015 LEFT HIP REVISED ON (B)(6) 2019 DUE MULTIPLE HIP DISLOCATION. THE FEMORAL STEM ORIGINALLY USED WAS A PROFEMUR Z CLASSIC SIZE 5 SHORT STRAIGHT NECK AND FEMORAL HEAD WAS A BIOLOX DELTA 28MM S, DOUBLE MOBILITY POLYETHYLENE LINER WAS USED. ONLY THE FEMORAL HEAD AND LINER WERE REVISED THERE IS NO FURTHER DATA ON WHAT DEVICES WERE IMPLANTED AFTER REVISION SURGERY.
Patient problems: Insufficient Information
MAUDE report 21316036 ↗
Other Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented devices
- NA 1365-51-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented753 reports
- NA 1365-50-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented412 reports
- ARTICUL/EZE 1365-21-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented1 recall280 reports
- ARTICUL/EZE 1365-11-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented1 death262 reports
- LFIT 6260-9-236Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/polymer, cemented256 reports
- PINNACLE GRIPTION 1217-32-052Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/polymer, cemented2 deaths239 reports
- ELEOS™ 25002111EOnkos Surgical, Inc. · Prosthesis, hip, semi-constrained, metal/polymer, cemented3 deaths230 reports
- Novation 130-36-52Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented2 recalls124 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page