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S-ROM 56-3624Recalls & reported problems

Depuy Orthopaedics, Inc. · S-ROM Total Hip System FEMORAL STEM Standard 36 STD NECK +12 11/13 TAPER 24x19x175 Lateral · Class 3 · Implant

All models of S-ROM (92)

Data updated Oct 18, 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 10603295178255), received between Aug 20, 2019 and Aug 20, 2019 — 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 18, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • No Code Available1
  • Pain1
  • Test Result1

Recent adverse event reports

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

  • InjuryAug 20, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    AFTER REVIEW OF MEDICAL RECORDS PATIENT WAS REVISED DUE TO PAIN, ELEVATED METAL IONS AND DISLOCATION. DOI: (B)(6) 2007, DOR: (B)(6) 2013, RIGHT HIP.

    Patient problems: No Code Available; Pain; Test Result

    MAUDE report 8910084 ↗

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

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

Sources and updates

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