DURALOC 1249-58-000Recalls & reported problems

Summary

The FDA's MAUDE database contains 14 adverse event reports that list this exact device (DI 10603295019794), received between Apr 19, 2018 and Aug 7, 2025 — classified as 14 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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 14 most recent of 14 reports, in the reporter's own words as published by the FDA.

• InjuryAug 7, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT WAS REVISED FOR CERAMIC HEAD AND POLY LINER EXCHANGE BECAUSE OF INFECTION. DOI: UNKNOWN, DOR: (B)(6) 2025, AFFECTED SIDE: UNKNOWN HIP.

  Patient problems: Unspecified Infection

  MAUDE report 22744274 ↗
• InjuryFeb 29, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT WAS REVISED DUE TO PAINFUL HIP. IT WAS UNKNOWN, IF THERE WAS A SURGICAL DELAY. DOI- UNKNOWN DOR- (B)(6) 2024 AFFECTED SIDE- UNKNOWN HIP.

  Patient problems: Pain

  MAUDE report 18808948 ↗
• InjuryJan 5, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT WAS REVISED DUE TO PAIN. DOI: UNKNOWN. DOR: (B)(6) 2022. AFFECTED SIDE: UNKNOWN HIP.

  Patient problems: Pain

  MAUDE report 16103664 ↗
• InjuryNov 16, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE PATIENT WAS REVISED DUE TO UNSTABLE AND HIP PAIN. DOI: UNKNOWN, DOR: (B)(6) 2021, AFFECTED SIDE: RIGHT SIDE.

  Patient problems: Joint Laxity; Pain

  MAUDE report 12822122 ↗
• InjuryNov 9, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE PATIENT WAS REVISED DUE TO ACUTE INFECTION. ORIGINAL IMPLANT DATE UNKNOWN. NO SURGICAL DELAY. DOI: UNKNOWN; DOR: (B)(6) 2021; AFFECTED SIDE: UNKNOWN.

  Patient problems: Unspecified Infection

  MAUDE report 12777905 ↗
• InjurySep 2, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE PATIENT WAS REVISED DUE TO INSTABILITY. DOI: UNKNOWN. DOR: (B)(6) 2021. AFFECTED SIDE: UNKNOWN HIP.

  Patient problems: Joint Laxity

  MAUDE report 12415434 ↗
• InjuryJul 6, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS STATED THAT PATIENT REPORTED PAIN. DOI: (B)(6) 2001 DOR: (B)(6) 2021 RIGHT HIP.

  Patient problems: Pain

  MAUDE report 12122203 ↗
• InjuryMay 10, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT PRESENTED WITH AN UNSTABLE HIP. SURGEON REMOVED LINER AND HEAD AND REPLACED WITH A CONSTRAINED LINER AND NEW RING AND HEAD. THIS WAS REVISED LAST YEAR (B)(6) 2020. DOI: (B)(6) 2020 - DOR: (B)(6) 2021 (RIGHT HIP).

  Patient problems: Joint Laxity

  MAUDE report 11797576 ↗
• InjuryFeb 26, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE PATIENT WAS REVISED DUE TO PAIN. NO SURGICAL DELAY. DOI: UNKNOWN, DOR: (B)(6) 2021, LEFT HIP.

  Patient problems: Pain

  MAUDE report 11389147 ↗
• InjuryJan 8, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE SURGEON PERFORMED A REVISION DUE TO AN INFECTED RIGHT HIP. THE PATIENT HAD A ZIMMER STEM AND HEAD IN SITU, AND A DEPUY CUP AND LINER (DETAILS UNKNOWN). IN THIS OPERATION, THE ENDURON LINER AND DURALOC LOCKING RING WERE REMOVED AND REPLACED BY ZIMMER PRODUCTS. THE DEPUY ACETABULAR CUP WAS NOT REMOVED. EXACT DATE AND SURGEON OF THE ORIGINAL OPERATION IS UNKNOWN, BUT THE STEM AND HEAD WERE REVISED TO ZIMMER IMPLANTS IN LATE 2000 FOLLOWING A FRACTURE (EXACT DATE UNKNOWN). THE SURGEON WAS UNABLE TO PROVIDE FURTHER DETAILS.

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

  MAUDE report 11141040 ↗
• InjuryJun 19, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT HAS HAD NUMEROUS SURGERIES, NUMEROUS REVISIONS. THE PATIENT HAS A CHRONIC INFECTION, AND THE CABLES ON THE FEMUR ARE CAUSING HIM PAIN. THE SURGEON DID NONE OF THE SURGERIES, BUT HE IS REMOVING THE CABLES, WASHING OUT AND CHANGING THE HEAD AND CONSTRAINED LINER. DOI: UNKNOWN. DOR: (B)(6) 2020; AFFECTED SIDE: UNKNOWN.

  Patient problems: No Code Available; Pain; Unspecified Infection

  MAUDE report 10173900 ↗
• InjuryOct 12, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT WAS REVISED DUE TO HIP PAIN.

  Patient problems: No Code Available; Pain

  MAUDE report 7961511 ↗
• InjuryMay 3, 2018Insufficient Device Problem Information; Insufficient Device Problem Information

  THE PATIENT WAS REVISED TO ADDRESS PAIN. DOI: (B)(6), 2000; DOR: (B)(6) 2018; RIGHT HIP.

  Patient problems: Not Applicable; Pain

  MAUDE report 7483840 ↗
• InjuryApr 19, 2018Insufficient Device Problem Information; Insufficient Device Problem Information

  PATIENT WAS REVISED TO ADDRESS PAIN. DOI: (B)(6) 2015; DOR: (B)(6) 2018; RIGHT HIP.

  Patient problems: Not Applicable; Pain

  MAUDE report 7442556 ↗