S-ROM 56-3122LRecalls & reported problems
Depuy Orthopaedics, Inc. · S-ROM Total Hip System FEMORAL STEM Left Long 36 STD NECK +8 11/13 TAPER 22x17x230 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 10603295177876), received between Apr 5, 2024 and Apr 5, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Degraded” (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.
Reports received per month
Most reported problems
Device problems
- Degraded1
Patient problems
- Foreign Body Reaction1
- Hypersensitivity/Allergic reaction1
- Inflammation1
- Osteolysis1
- Pain1
- Swelling/ Edema1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryApr 5, 2024Degraded; Degraded
MEDICAL RECORDS RECEIVED. DOI: (B)(6) 2007: MALE PATIENT WITH A HISTORY OF LEFT HIP FEMORAL FRACTURE, LEFT HIP COMPETITOR ORIF, LEFT HIP COMPETITOR THA, ACETABULAR AND FEMORAL OSTEOLYSIS, AND CHRONIC SEPSIS INFECTION RECEIVED A DEPUY MOM REVISION THA AS STAGE 2 TREATMENT OF INFECTION. THE ACETABULAR CUP WAS SECURED WITH A DOME SCREW AND THE ACETABULAR OSTEOLYSIS REQUIRED BONE GRAFTING. THE PREVIOUS FEMORAL FRACTURE SITE WAS PARTIALLY HEALED AND REQUIRED A LARGER BONE CUT AND THE USE OF AN S-ROM STEM AND SLEEVE. THE SURGEONS NOTED THERE WAS SOME SHORTENING OF THE LEFT LEG BECAUSE OF THE PREEXISTING FRACTURE CAUSED BY AN MVA. THE PROCEDURE WAS COMPLETED WITHOUT COMPLICATIONS. CT SCAN AND PREOPERATIVE TESTING (B)(6) 2024: A MALE PATIENT IS REFERRED FOR REVISION SURGERY AFTER FAILED ATTEMPTS AT TREATING CHRONIC LEFT HIP PAIN. PREOPERATIVE ASPIRATION DOES NOT DETECT ELEVATED SERUM OR SYNOVIAL HEAVY METAL IONS BUT DOES DETECT ELEVATED INFLAMMATORY MARKERS. CT SCANS IDENTIFY A LARGE PSEUDOTUMOR AS WELL AS EXTENSIVE ACETABULAR AND FEMORAL OSTEOLYSIS. THESE WERE PREEXISTING EVENTS AND ARE PART OF THE TREATMENT OF REVISION CAPTURED ON (B)(4).
Patient problems: Foreign Body Reaction; Hypersensitivity/Allergic reaction; Inflammation; Osteolysis; Pain; Swelling/ Edema
MAUDE report 19051280 ↗
Other Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented devices
- BIOLOX DELTA 1365-36-310Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented839 reports
- BIOLOX DELTA 1365-36-320Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented643 reports
- PINNACLE POROCOAT 1217-22-052Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented335 reports
- PINNACLE POROCOAT 1217-22-054Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented263 reports
- BIOLOX DELTA 1365-36-330Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented255 reports
- PINNACLE POROCOAT 1217-22-050Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented253 reports
- PINNACLE POROCOAT 1217-22-056Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented220 reports
- SUMMIT POROCOAT 1570-11-120Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented1 death204 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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