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S-ROM ZTT 55-0727Recalls & reported problems

Depuy Orthopaedics, Inc. · S-ROM Total Hip System ZTT Oversize Proximal Sleeve POROUS COATED 20 F SML FITS: 18 x 13 STEM Cone: F Triangle: SML 18 INTERNAL DIAMETER · Class 3 · Implant

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 10603295175575), received between Jan 16, 2020 and Jan 16, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Loss of Osseointegration” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Loss of Osseointegration1
  • Osseointegration Problem1

Patient problems

  • Inadequate Osseointegration1
  • No Code Available1

Recent adverse event reports

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

  • InjuryJan 16, 2020Loss of Osseointegration; Osseointegration Problem; Loss of Osseointegration; Osseointegration Problem

    THE PATIENT WAS REVISED TO ADDRESS LOOSENING OF THE SROM STEM AT BONE TO IMPLANT INTERFACE. DOI: (B)(6) 2019; DOR: (B)(6) 2020 (RIGHT HIP).

    Patient problems: Inadequate Osseointegration; No Code Available

    MAUDE report 9596625 ↗

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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