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DURALOC 1245-44-503Recalls & reported problems

Depuy Orthopaedics, Inc. · DURALOC ACETABULAR CUP SYSTEM BANTAM ACETABULAR SHELL 44mm OD · Class 2 · Implant

All models of DURALOC (93)

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 10603295019435), received between Jul 8, 2021 and Jul 8, 2021 — 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

  • Pain1

Recent adverse event reports

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

  • InjuryJul 8, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THIS PATIENT'S PRIMARY HIP WAS REVISED DUE TO POLY WEAR AND SCIATIC NERVE PAIN. HER PRIMARY ARTICUL/EZE FEMORAL HEAD, DURALOC BANTAM CUP, AND DURALOC ACETABULAR LINER WERE REMOVED AND REPLACED BY A LARGER BIOLOX DELTA CERAMIC FEMORAL HEAD,A LARGER PINNACLE CUP, AND AN ALTRX LINER. DOI: (B)(6) 2001, DOR: (B)(6) 2021, AFFECTED SIDE: RIGHT HIP.

    Patient problems: Pain

    MAUDE report 12135403 ↗

Other PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED devices

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Sources and updates

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