DURALOC 1242-16-527Recalls & reported problems
Depuy Orthopaedics, Inc. · DURALOC ACETABULAR CUP SYSTEM CONSTRAINED LINER 32mm ID 56/68mm OD · Class 2 · Implant
All models of DURALOC (93)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 7
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 10603295019206), received between Dec 27, 2017 and Jul 19, 2023 — classified as 7 injuries.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (7 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 16, 2026.
Most reported problems
Device problems
- Device Dislodged or Dislocated7
- Naturally Worn1
Patient problems
- Joint Dislocation6
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- No Code Available1
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
InjuryJul 19, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated
IT WAS REPORTED THAT PATIENT HAD A POLY AND HEAD EXCHANGE DUE TO DISLOCATION. DOI: UNKNOWN. DOR: (B)(6) 2023. AFFECTED SIDE: RIGHT HIP.
Patient problems: Joint Dislocation
MAUDE report 17351550 ↗InjuryMay 5, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated
PATIENT WAS REVISED DUE TO THE DISLOCATION OF HEAD AND LINER AND WERE REPLACED. NEW 28 HEAD 958840 BROKE WHEN REMOVING. UNKNOWN IF ANY LOOSENING. UNKNOWN IF ANY SURGICAL DELAY. DOI: (B)(6) 2020. DOR: (B)(6) 2022. AFFECTED SIDE: LEFT HIP.
Patient problems: Joint Dislocation
MAUDE report 14287763 ↗InjuryMay 26, 2021Device Dislodged or Dislocated; Device Dislodged or Dislocated
IT WAS REPORTED THAT PATIENT HAD PREVIOUS TOTAL HIP SURGERY AND HAD BEEN DISLOCATING. SURGEON REMOVED A DURALOC CUP WITH A CONSTRAINED LINER AND A 32 8.5 METAL HEAD. REPLACED WITH A COMPETITOR DUAL MOBILITY CONSTRUCT AND A DEPUY HEAD BALL. DOI: UNKNOWN DOR: (B)(6) 2021 RIGHT HIP.
Patient problems: Joint Dislocation
MAUDE report 11887218 ↗InjuryMay 20, 2021Device Dislodged or Dislocated; Device Dislodged or Dislocated
ON (B)(6) 2021 SURGEON REMOVED A DURALOC CONSTRAINED LINER, A DURALOC DYNAMIC LOCKING RING, AND A TOTAL HIP BALL FEMORAL HEAD. THESE WERE REPLACED WITH IDENTICAL NEW COMPONENTS. REASON FOR REVISION: DISLOCATION. THE LARGE METAL LOCKING RING WHICH IS USUALLY CONSTRAINED WITHIN THE LINER HAD COMPLETELY POPPED OUT OF THE LINER ITSELF. X-RAYS AND OTHER OPERATIVE NOTES UNAVAILABLE.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 11857374 ↗InjuryNov 27, 2018Device Dislodged or Dislocated; Naturally Worn; Device Dislodged or Dislocated; Naturally Worn
PATIENT WAS REVISED DUE TO DISLOCATION.
Patient problems: Joint Dislocation; No Code Available
MAUDE report 8105585 ↗InjuryDec 29, 2017Device Dislodged or Dislocated; Device Dislodged or Dislocated
PATIENT WAS REVISED FOR ACUTE DISLOCATION. THE SAME IMPLANTS WERE REIMPLANTED.
Patient problems: Joint Dislocation
MAUDE report 7154022 ↗InjuryDec 27, 2017Device Dislodged or Dislocated; Device Dislodged or Dislocated
PATIENT WAS REVISED FOR DISLOCATION. THE OLD LINER AND HEAD WERE REMOVED AND NEW LINER AND HEAD WERE IMPLANTED. PATIENT CONSEQUENCE?: NO. IS THE INFORMATION BEING SUBMITTED FOR THIS COMPLAINT ALL THE DETAILS THAT ARE KNOWN/AVAILABLE REGARDING THIS EVENT?: YES.
Patient problems: Joint Dislocation
MAUDE report 7147440 ↗
Other Prosthesis, hip, constrained, cemented or uncemented, metal/polymer devices
- Novation 134-36-45Exactech, Inc. · Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer2 recalls0 reports
- PINNACLE 1218-28-650Depuy Orthopaedics, Inc. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer89 reports
- Trident 690-00-28FHowmedica Osteonics Corp. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 recall37 reports
- Trident 690-00-22EHowmedica Osteonics Corp. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 recall36 reports
- PINNACLE 1218-32-652Depuy Orthopaedics, Inc. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer75 reports
- Trident 690-00-22DHowmedica Osteonics Corp. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 recall22 reports
- PINNACLE 1218-32-654Depuy Orthopaedics, Inc. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer70 reports
- Trident 69-2850Howmedica Osteonics Corp. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 recall11 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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