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EMPHASYS 4741-03-200Recalls & reported problems

Depuy (Ireland) · EMPHASYS 12/14 FEMORAL STEM COLLARED STANDARD OFFSET HA COATED 3 SO · Class 2 · Implant

All models of EMPHASYS (109)

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 10603295505426), received between Nov 16, 2022 and Nov 16, 2022 — classified as 1 injury.

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

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Fall1
  • Limb Fracture1

Recent adverse event reports

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

  • InjuryNov 16, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT PATIENT FELL, BROKE THEIR GREATER TROCH. SURGEON FIXED TROCH AND REVISED TO DUAL MOBILITY CONSTRUCT. THERE WAS NO SURGICAL DELAY. DOI: (B)(6) 2022, DOR: (B)(6) 2022, AFFECTED SIDE- RIGHT HIP.

    Patient problems: Fall; Limb Fracture

    MAUDE report 15803996 ↗

Other Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented devices

All Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented devices →

Sources and updates

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