DURALOCRecalls & reported problems across all models
Depuy Orthopaedics, Inc. · 93 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1,262
- Deaths reported
- 1
- Injuries reported
- 495
- Recalls
- 0
We found 93 models of DURALOC by Depuy Orthopaedics, Inc. in the FDA's device registry (GUDID). Together they are named in 1,262 adverse event reports in the FDA's MAUDE database, received between Jun 28, 2017 and Sep 18, 2026 — classified as 1 death, 495 injuries, 766 malfunctions.
The most frequently reported specific device problem is “Naturally Worn” (375 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported DURALOC problems
Device problems
- Naturally Worn375
- Break282
- Adverse Event Without Identified Device or Use Problem145
- Crack144
- Device Dislodged or Dislocated132
- Material Deformation102
- Material Twisted/Bent87
- Device-Device Incompatibility80
Patient problems
- No Clinical Signs, Symptoms or Conditions412
- No Consequences Or Impact To Patient271
- Insufficient Information153
- No Code Available152
- Joint Dislocation133
- Pain124
- No Information48
- Not Applicable43
DURALOC models
93 models, most reported first. Each model has its own page with its reports, recalls and device details.
- DURALOC 2360-71-000IMPACTOR716 reports
- DURALOC 1220-28-148Prosthesis, hip, semi-constrained, metal/polymer, cemented42 reports
- DURALOC 1220-28-150Prosthesis, hip, semi-constrained, metal/polymer, cemented38 reports
- DURALOC 1220-32-152PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED29 reports
- DURALOC 1220-32-156PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED19 reports
- DURALOC 1220-28-154PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED17 reports
- DURALOC 1241-46-526PROSTHESIS, ELBOW, SEMI-CONSTRAINED, CEMENTED17 reports
- DURALOC 1220-32-154PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED16 reports
- DURALOC 1241-10-527Prosthesis, hip, constrained, cemented or uncemented, metal/polymer16 reports
- DURALOC 1249-58-000PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED14 reports
- DURALOC 1249-54-000PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED13 reports
- DURALOC 1249-56-000PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED13 reports
- DURALOC 1220-28-152Prosthesis, hip, semi-constrained, metal/polymer, cemented12 reports
- DURALOC 1249-52-000PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED11 reports
- DURALOC 1220-28-156Prosthesis, hip, semi-constrained, metal/polymer, cemented10 reports
- DURALOC 1220-32-158PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED10 reports
- DURALOC 1242-12-527Prosthesis, hip, constrained, cemented or uncemented, metal/polymer10 reports
- DURALOC 1249-60-000PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED10 reports
- DURALOC 1249-48-000PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED8 reports
- DURALOC 1220-28-056Prosthesis, hip, semi-constrained, metal/polymer, cemented7 reports
- DURALOC 1220-28-160PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED7 reports
- DURALOC 1220-32-052PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED7 reports
- DURALOC 1220-32-452Prosthesis, hip, semi-constrained, metal/polymer, cemented7 reports
- DURALOC 1220-36-458PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED7 reports
- DURALOC 1220-36-460PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED7 reports
- DURALOC 1220-36-560PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED7 reports
- DURALOC 1242-14-527Prosthesis, hip, constrained, cemented or uncemented, metal/polymer7 reports
- DURALOC 1242-16-527Prosthesis, hip, constrained, cemented or uncemented, metal/polymer7 reports
- DURALOC 2220-36-554TEMPLATE7 reports
- DURALOC 1220-28-050Prosthesis, hip, semi-constrained, metal/polymer, cemented6 reports
- DURALOC 1220-28-052PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED6 reports
- DURALOC 1220-28-158Prosthesis, hip, semi-constrained, metal/polymer, cemented6 reports
- DURALOC 1220-36-456PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED6 reports
- DURALOC 1220-36-556PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED6 reports
- DURALOC 1242-18-527Prosthesis, hip, constrained, cemented or uncemented, metal/polymer6 reports
- DURALOC 1220-28-048Prosthesis, hip, semi-constrained, metal/polymer, cemented5 reports
- DURALOC 1220-32-160PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED5 reports
- DURALOC 1220-36-554PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED5 reports
- DURALOC 1220-36-558PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED5 reports
- DURALOC 1242-20-527Prosthesis, hip, constrained, cemented or uncemented, metal/polymer5 reports
- DURALOC 1249-50-000PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED5 reports
- DURALOC 1249-62-000PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED5 reports
- DURALOC 2220-36-558TEMPLATE5 reports
- DURALOC 1220-32-054PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED4 reports
- DURALOC 1220-36-454PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED4 reports
- DURALOC 1220-36-562PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED4 reports
- DURALOC 1241-08-527Prosthesis, hip, constrained, cemented or uncemented, metal/polymer4 reports
- DURALOC 1241-16-527Prosthesis, hip, constrained, cemented or uncemented, metal/polymer4 reports
- DURALOC 1242-24-527Prosthesis, hip, constrained, cemented or uncemented, metal/polymer4 reports
- DURALOC 1220-28-054Prosthesis, hip, semi-constrained, metal/polymer, cemented3 reports
- DURALOC 1220-32-058PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 death3 reports
- DURALOC 1220-32-162PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED3 reports
- DURALOC 1241-14-527Prosthesis, hip, constrained, cemented or uncemented, metal/polymer3 reports
- DURALOC 1249-66-000PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED3 reports
- DURALOC 2220-36-458TEMPLATE3 reports
- DURALOC 1220-28-058Prosthesis, hip, semi-constrained, metal/polymer, cemented2 reports
- DURALOC 1220-28-162PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 reports
- DURALOC 1220-28-448Prosthesis, hip, semi-constrained, metal/polymer, cemented2 reports
- DURALOC 1220-28-450PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 reports
- DURALOC 1220-32-056PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 reports
- DURALOC 1220-32-060PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 reports
- DURALOC 1220-32-062PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 reports
- DURALOC 1220-32-456Prosthesis, hip, semi-constrained, metal/polymer, cemented2 reports
- DURALOC 1220-36-466PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 reports
- DURALOC 1220-36-564PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 reports
- DURALOC 1241-20-527Prosthesis, hip, constrained, cemented or uncemented, metal/polymer2 reports
- DURALOC 1241-44-526PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER2 reports
- DURALOC 1242-22-527Prosthesis, hip, constrained, cemented or uncemented, metal/polymer2 reports
- DURALOC 1242-26-527Prosthesis, hip, constrained, cemented or uncemented, metal/polymer2 reports
- DURALOC 2220-36-464TEMPLATE2 reports
- DURALOC 1220-28-060PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- DURALOC 1220-28-062Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- DURALOC 1220-32-064PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- DURALOC 1220-32-166PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- DURALOC 1220-32-454Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- DURALOC 1220-32-458PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- DURALOC 1220-36-462PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- DURALOC 1220-36-566PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- DURALOC 1241-12-527Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 report
- DURALOC 1241-22-527Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 report
- DURALOC 1241-38-526PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- DURALOC 1241-40-526PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- DURALOC 1241-42-526PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- DURALOC 1245-38-503Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- DURALOC 1245-44-503PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- DURALOC 1249-64-000PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- DURALOC 2220-36-456TEMPLATE1 report
- DURALOC 2220-36-460TEMPLATE1 report
- DURALOC 2220-36-556TEMPLATE1 report
- DURALOC 2220-36-566TEMPLATE1 report
- DURALOC 2247-16-000TEMPLATE1 report
- DURALOC 2248-08-000TEMPLATE1 report
- DURALOC 2999-66-393IMPACTOR1 report
Recent DURALOC adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjurySep 18, 2026Naturally Worn
It was reported that duraloc liner poly wear, taking out 52 lipped liner, 52 locking ring, 28 1.5 head. No information on when it was implanted. Allpieces were retrieved. No delay in case.Affected Side: Left.
Patient problems: Insufficient Information
MAUDE report 50819940 ↗InjurySep 17, 2026Naturally Worn
It was reported that the insert worn was out.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50804268 ↗InjurySep 17, 2026Naturally Worn
It was reported that the insert was worn out- right.
Patient problems: Insufficient Information
MAUDE report 50804236 ↗MalfunctionSep 17, 2026Naturally Worn
It was reported that there was a worn Duraloc PE Inlay. There was no patient harm.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50804006 ↗InjurySep 16, 2026Naturally Worn
Patient problems: Insufficient Information
MAUDE report 50795302 ↗InjurySep 16, 2026Naturally Worn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50795178 ↗InjurySep 16, 2026Naturally Worn
Patient problems: Insufficient Information
MAUDE report 50794960 ↗InjurySep 16, 2026Naturally Worn
It was reported the Inserts were worn out on both sides.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50788375 ↗MalfunctionSep 14, 2026Naturally Worn
It was reported that post hip implant surgical procedure it was observed that the insert was worn out - right.
Patient problems: Insufficient Information
MAUDE report 50755627 ↗MalfunctionSep 14, 2026Naturally Worn
It was reported the post hip implant surgical procedure it was observed that the insert was worn out - right.
Patient problems: Insufficient Information
MAUDE report 50755530 ↗MalfunctionSep 14, 2026Naturally Worn
It was reported the post right hip surgery implant surgical procedure it was observed that the inserts were worn out-both on both sides.
Patient problems: Insufficient Information
MAUDE report 50755216 ↗MalfunctionSep 11, 2026Naturally Worn
It was reported that a worn-out left insert had been observed. The issue related to polyethylene wear associated with long-term use and not to the locking ring itself. All available information has been disclosed.
Patient problems: Insufficient Information
MAUDE report 50736840 ↗MalfunctionSep 11, 2026Naturally Worn
It was reported that a worn-out right insert had been observed. It had worn out over time. The device was still implanted. The issue related to polyethylene wear associated with long-term use and not to the locking ring itself. All available information has been disclosed.
Patient problems: Insufficient Information
MAUDE report 50736669 ↗MalfunctionSep 11, 2026Naturally Worn
It was reported that a worn-out left insert during a hip surgery. The device was still implanted. The issue related to polyethylene wear associated with long-term use and not to the locking ring itself. All available information has been disclosed.
Patient problems: Insufficient Information
MAUDE report 50736562 ↗InjuryAug 28, 2026Device Dislodged or Dislocated
It was reported that the patient presented dislocated for a fall. Head and liner exchange was made and patient was stable with proper leg length.DOI: (b)(6) 2023.DOR: (b)(6) 2026.Affected side: Right.
Patient problems: Fall; Joint Dislocation
MAUDE report 50505964 ↗
Other Depuy Orthopaedics, Inc. products
- PINNACLE ALTRX98 models · 5,631 reports
- BIOLOX DELTA40 models · 4,995 reports · 1 recall
- PINNACLE182 models · 4,587 reports
- QUICKSET7 models · 3,790 reports
- PINNACLE POROCOAT38 models · 2,112 reports
- SUMMIT POROCOAT20 models · 1,646 reports
- PINNACLE GRIPTION57 models · 1,608 reports
- SUMMIT53 models · 697 reports
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- 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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