DURALOC 1249-52-000Recalls & reported problems

Summary

The FDA's MAUDE database contains 11 adverse event reports that list this exact device (DI 10603295019763), received between Jun 4, 2018 and Nov 3, 2025 — classified as 11 injuries.

The most frequently reported specific device problem is “Fracture” (2 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 11 most recent of 11 reports, in the reporter's own words as published by the FDA.

• InjuryNov 3, 2025Naturally Worn; Naturally Worn

  IT WAS REPORTED A REVISION SURGERY OCCURRED BECAUSE THE LEFT HIP DURALOC MARATHON ACETABULAR LINER AND LOCKING RING ARE WORN OUT. ORIGINAL IMPLANT DATE WAS (B)(6) 2010.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23452872 ↗
• InjuryJun 26, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THERE WAS A WORN OUT PE ON THE RIGHT HIP JOINT. PATIENT IS IN PAIN, REVISION SURGERY IS NEEDED.

  Patient problems: Pain

  MAUDE report 22337941 ↗
• InjuryJun 23, 2025Fracture; Fracture

  IT WAS REPORTED THAT THE DURALOC LOCKING RING WAS BROKEN. HIP GOT DISLOCATED. DOI: UNK. DOR: (B)(6) 2025. AFFECTED AREA: LEFT HIP.

  Patient problems: Insufficient Information

  MAUDE report 22309432 ↗
• InjuryJun 10, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  ADDITIONAL INFORMATION RECEIVED: REVISION SURGERY HAS NOT BEEN PERFORMED YET, AS THE NEW IMPLANT NEEDS TO BE MANUFACTURED FIRST.

  Patient problems: Pain

  MAUDE report 22178644 ↗
• InjuryDec 26, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT PATIENT UNDERWENT REVISION SURGERY ON (B)(6) 2024, DUE TO PAIN. DOCTOR REVISED THE POLY AND HEAD BALL. NO INFECTION PRESENT. NO DELAY IN SURGERY. DOI: UNKNOWN. DOR: (B)(6) 2024. AFFECTED SIDE: LEFT KNEE.

  Patient problems: Pain

  MAUDE report 21019254 ↗
• InjuryAug 30, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT WAS REVISED DUE TO INFECTION. NO SURGICAL DELAY WAS REPORTED. DOI: UNKNOWN. DOR: (B)(6) 2022. AFFECTED SIDE: RIGHT HIP.

  Patient problems: Unspecified Infection

  MAUDE report 15324031 ↗
• InjuryOct 19, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE PATIENT WAS REVISED DUE TO INFECTION. DOI: (B)(6) 2001, DOR: (B)(6) 2021, AFFECTED SIDE: RIGHT HIP.

  Patient problems: Unspecified Infection

  MAUDE report 12656127 ↗
• InjuryFeb 23, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE PATIENT WAS REVISED TO ADDRESS HIP PAIN. DOI: UNKNOWN, DOR: (B)(6) 2021, AFFECTED SIDE: LEFT HIP.

  Patient problems: Pain

  MAUDE report 11366886 ↗
• InjuryDec 17, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE PATIENT WAS REVISED TO ADDRESS PAINFUL HIP DUE TO WORN POLY. ORIGINAL IMPLANT DATE UNKNOWN.

  Patient problems: No Code Available; Pain

  MAUDE report 8168694 ↗
• InjuryJul 24, 2018Insufficient Device Problem Information; Insufficient Device Problem Information

  THE PATIENT WAS REVISED TO ADDRESS PAIN. DOI: (B)(6) 1992; DOR: (B)(6) 2018; RIGHT HIP.

  Patient problems: Pain

  MAUDE report 7713802 ↗
• InjuryJun 4, 2018Fracture; Fracture

  DER STATES THAT THE LOCKING MECHANISM FOR THE DURALOC CUP WAS BROKEN INTO PIECES. IT WAS ALSO REPORTED THAT THE LINER WAS LOOSENED. DOI: UNKNOWN; DOR: (B)(6) 2018; LEFT HIP.

  Patient problems: Not Applicable

  MAUDE report 7566192 ↗