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S-ROM ZTT 55-0546Recalls & reported problems

Depuy (Ireland) · S-ROM Modular Hip System ZTT Proximal Sleeve POROUS COATED 22 F LRG FITS: 22 x 17 STEM Cone: F Triangle: LRG · Class 3 · Implant

All models of S-ROM ZTT (36)

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 10603295175414), received between Sep 19, 2018 and Sep 19, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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

  • Insufficient Device Problem Information1

Patient problems

  • Infarction, Cerebral1
  • Myocardial Infarction1

Recent adverse event reports

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

  • InjurySep 19, 2018Insufficient Device Problem Information; Insufficient Device Problem Information

    PPF ALLEGES STROKE/HEART ATTACK AFTER REVISION. NO REVISION NOTE PROVIDED. DOI: (B)(6) 2011; DOR: NONE REPORTED; (RIGHT HIP).

    Patient problems: Infarction, Cerebral; Myocardial Infarction

    MAUDE report 7890155 ↗

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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