S-ROM MARATHON 1220-72-132Recalls & reported problems

Summary

The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 10603295015901), received between Nov 11, 2017 and Jul 10, 2023 — classified as 8 injuries, 1 malfunction.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (3 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.

Most reported problems

Recent adverse event reports

The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.

• InjuryJul 10, 2023Naturally Worn; Naturally Worn

  PATIENT WAS REVISED DUE TO POLY WEAR OF ACETABULAR LINER. DOI: UNKNOWN. DOR: (B)(6) 2023. AFFECTED SIDE: LEFT HIP.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17287686 ↗
• InjuryAug 24, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT WAS REVISED DUE TO PAINFUL LEFT HIP. PREVIOUS SURGERY DATE AND LOCATION IS UNKNOWN. DOI: UNKNOWN. DOR: (B)(6) 2022. AFFECTED SIDE: LEFT HIP.

  Patient problems: Pain

  MAUDE report 15282613 ↗
• MalfunctionFeb 11, 2021Difficult to Insert; Difficult to Insert

  IT WAS REPORTED THAT THE SURGEON WAS UNABLE TO GET THE REPLACEMENT INSERT TO PROPERLY ENGAGE AFTER SEVERAL ATTEMPTS (CATALOG # 122072132, LOT # 8506054). HE THEN SELECTED A 32 +3 10 DEGREE L SERIES INSERTS. AFTER SEVERAL ATTEMPTS HE WAS ABLE TO GET IT IMPLANTED AND THE 3 REPLACEMENT SCREWS WERE PLACED. I WAS UNABLE TO RETRIEVE THE ORIGINAL REPLACEMENT INSERT. DOE: (B)(6) 2021. RIGHT HIP.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11315840 ↗
• InjuryNov 16, 2020Naturally Worn; Naturally Worn

  IT WAS REPORTED THAT THE PATIENT HAD REVISION FOR POLYETHYLENE WEAR. LINER EXCHANGE. FEMORAL COMPONENT HAD LOOSENING ALSO. DOI: UNKNOWN DOR: (B)(6) 2020 RIGHT HIP.

  Patient problems: No Code Available

  MAUDE report 10845157 ↗
• InjuryJun 24, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT PATIENT HAD AN SROM CUP PLACED DURING AN ACETABULAR REVISION MANY YEARS AGO. PREVIOUS RECORDS ARE UNAVAILABLE. THERE IS A ZIMMER STEM IN NOW. HIP BECAME INFECTED AND PATIENT HAD A HEAD /LINER EXCHANGE WITH EXTENSIVE DEBRIDEMENT AND IRRIGATION. DOI: UNKNOWN, DOR: (B)(6) 2020, AFFECTED SIDE: RIGHT HIP.

  Patient problems: No Code Available; Unspecified Infection

  MAUDE report 10191115 ↗
• InjuryNov 1, 2019Naturally Worn; Naturally Worn

  IT WAS REPORTED THAT THE PATIENT HAD EXCHANGED OF POLY AND HEAD FOR POLY WEAR. DOI: (B)(6) 2001; DOR: (B)(6) 2019; RIGHT HIP.

  Patient problems: No Code Available

  MAUDE report 9267513 ↗
• InjuryJun 6, 2019Device Dislodged or Dislocated; Device Dislodged or Dislocated

  MEDICAL RECORDS INDICATE THAT THE PATIENT ALSO HAD PAIN AND HEMATOMA.

  Patient problems: Hematoma; Joint Dislocation; No Code Available; Pain

  MAUDE report 8674577 ↗
• InjuryFeb 5, 2018Device Dislodged or Dislocated; Device Dislodged or Dislocated

  PATIENT WAS REVISED TO ADDRESS DISLOCATION. DOI: UNKNOWN; DOR: (B)(6) 2018. LEFT HIP.

  Patient problems: Joint Dislocation

  MAUDE report 7240567 ↗
• InjuryNov 11, 2017Device Dislodged or Dislocated; Device Dislodged or Dislocated

  PATIENT WAS REVISED TO ADDRESS DISLOCATION.

  Patient problems: Joint Dislocation

  MAUDE report 7023381 ↗