Skip to content

S-ROM ZTT 55-0737Recalls & reported problems

Depuy Orthopaedics, Inc. · S-ROM Total Hip System ZTT Oversize Proximal Sleeve POROUS COATED 22 F SML FITS: 20 x 15 STEM Cone: F Triangle: SML 20 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 10603295175605), received between Feb 13, 2019 and Feb 13, 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

Recent adverse event reports

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

  • InjuryFeb 13, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THE ORIGINAL IMPLANT DATE IS UNKNOWN. PATIENT WAS SUFFERING FROM ANTERIOR THIGH PAIN. THE SURGEON DECIDED HE WANTED TO REMOVE THE S-ROM STEM, SLEEVE, AND 36MM HEAD AND IMPLANT A BOWED STRYKER RESTORATION STEM. HE DECIDED IT WAS BEST TO LEAVE THE PATIENTS ACETABULAR COMPONENTS. DOI: UNKNOWN; DOR: (B)(6) 2019; LEFT HIP.

    Patient problems: No Code Available; Pain

    MAUDE report 8336844 ↗

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

How reports and recalls are matched · Editorial policy · Report an error on this page