S-ROM MARATHON 1220-70-328Recalls & reported problems
Depuy Orthopaedics, Inc. · S-ROM MARATHON ACETABULAR LINER 28mm +3 10 DEGREES M SERIES · Class 3 · Implant
All models of S-ROM MARATHON (4)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 6
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10603295015857), received between Oct 23, 2017 and Apr 21, 2026 — classified as 6 injuries.
The most frequently reported specific device problem is “Naturally Worn” (4 reports).
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
- Naturally Worn4
- Device Dislodged or Dislocated3
Patient problems
- Joint Dislocation2
- No Code Available2
- Pain2
- Insufficient Information1
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
InjuryApr 21, 2026Naturally Worn
THAYER SCHOOL OF ENGINEERING AT DARTMOUTH FIRST REPORT OF RETRIEVALS FOR STATEMENT OF WORK 10 FOR Q1 OF 2026. DARTHMOUTH IS THE RESEARCH LOCATION, AND NOT THE FACILITY OF PLACEMENT. A DEPUY SYNTHES IMPLANT WAS REVISED AND REVIEWED FOR ANALYSIS. REASON FOR REVISION: PAIN. RETRIEVAL ANALYSIS IDENTIFIED LOOSENING OF THE CUP AT THE BONE TO IMPLANT INTERFACE AND METAL WEAR OF THE CUP AS WELL AS WEAR OF THE POLY LINER.
Patient problems: Pain
MAUDE report 24942577 ↗InjuryApr 14, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated
THE PATIENT WAS REVISED DUE TO LOCKING PIN DISASSOCIATING. DOI: (B)(6) 2015. DOR: (B)(6) 2023. AFFECTED SIDE: LEFT HIP.
Patient problems: Insufficient Information
MAUDE report 16742435 ↗InjuryDec 17, 2020Naturally Worn; Naturally Worn
IT WAS REPORTED THAT THE DOCTOR REVISED FOR PAIN DUE TO WORN POLY. ORIGINAL IMPLANT DATE UNKNOWN. DOI: UNKNOWN. DOR: (B)(6) 2020. AFFECTED SIDE: LEFT HIP.
Patient problems: Pain
MAUDE report 11027561 ↗InjuryJun 7, 2019Naturally Worn; Naturally Worn
IT WAS REPORTED THAT THE PATIENT HAD A HEAD AND LINER EXCHANGE . POLY WEAR 2 SCREWS WERE REMOVED UNABLE TO IDENTIFY SIZE OR LOT. DOI: UNKNOWN; DOR: (B)(6) 2019, LEFT HIP.
Patient problems: No Code Available
MAUDE report 8678602 ↗InjuryMay 23, 2019Device Dislodged or Dislocated; Naturally Worn; Device Dislodged or Dislocated; Naturally Worn
IT WAS REPORTED THAT PATIENT HAD POLY WEAR & DISLOCATION. DOI: UNKNOWN; DOR: (B)(6) 2019; LEFT HIP.
Patient problems: Joint Dislocation; No Code Available
MAUDE report 8635914 ↗InjuryOct 23, 2017Device Dislodged or Dislocated; Device Dislodged or Dislocated
THE PATIENT WAS REVISED TO ADDRESS DISLOCATION AND LOOSENING OF THE CUP AT THE BONE TO IMPLANT INTERFACE.
Patient problems: Joint Dislocation
MAUDE report 6970505 ↗
Other Prosthesis, hip, semi-constrained (metal uncemented acetabular component) devices
- BIOLOX DELTA 1365-32-730Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained (metal uncemented acetabular component)93 reports
- RingLoc® Hip System 103531Biomet Orthopedics, LLC · Prosthesis, hip, semi-constrained (metal uncemented acetabular component)1 recall0 reports
- BIOLOX DELTA 1365-28-710Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained (metal uncemented acetabular component)43 reports
- ASPHERE 1365-52-100Depuy (Ireland) · Prosthesis, hip, semi-constrained (metal uncemented acetabular component)39 reports
- ASPHERE 1365-05-100Depuy (Ireland) · Prosthesis, hip, semi-constrained (metal uncemented acetabular component)29 reports
- ASPHERE 1365-06-100Depuy (Ireland) · Prosthesis, hip, semi-constrained (metal uncemented acetabular component)29 reports
- Taperloc Complete Micro Primary Femoral 51-107130Biomet Orthopedics, LLC · Prosthesis, hip, semi-constrained (metal uncemented acetabular component)23 reports
- Taperloc Complete Micro Primary Femoral 51-107120Biomet Orthopedics, LLC · Prosthesis, hip, semi-constrained (metal uncemented acetabular component)19 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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