ARTICUL/EZERecalls & reported problems across all models
Depuy (Ireland) · 26 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3,031
- Deaths reported
- 2
- Injuries reported
- 1,363
- Recalls
- 1
We found 26 models of ARTICUL/EZE by Depuy (Ireland) in the FDA's device registry (GUDID). Together they are named in 3,031 adverse event reports in the FDA's MAUDE database, received between Jul 9, 2013 and Sep 22, 2026 — classified as 2 deaths, 1,363 injuries, 1,666 malfunctions.
The most frequently reported specific device problem is “Scratched Material” (895 reports).
1 FDA recall record name at least one of these models by its device identifier.
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
ARTICUL/EZE recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- May 7, 2021Terminated
Fifty (50) individual units from Lot D20111130 were distributed with the incorrect part number and size etched on the product.
Z-1845-2021 · Root cause: Employee error · Recall details · FDA record ↗
Most reported ARTICUL/EZE problems
Device problems
- Scratched Material895
- Naturally Worn696
- Adverse Event Without Identified Device or Use Problem616
- Device Dislodged or Dislocated571
- Break360
- Material Deformation159
- Material Twisted/Bent139
- Insufficient Device Problem Information105
Patient problems
- No Clinical Signs, Symptoms or Conditions1,149
- Joint Dislocation567
- No Consequences Or Impact To Patient464
- No Code Available429
- Pain301
- Unspecified Infection288
- Joint Laxity107
- Not Applicable89
ARTICUL/EZE models
26 models, most reported first. Each model has its own page with its reports, recalls and device details.
- ARTICUL/EZE 1365-21-000Prosthesis, hip, semi-constrained, metal/polymer, cemented1 recall280 reports
- ARTICUL/EZE 2531-51-000TEMPLATE323 reports
- ARTICUL/EZE 2530-91-000TEMPLATE271 reports
- ARTICUL/EZE 1365-11-000Prosthesis, hip, semi-constrained, metal/polymer, cemented1 death262 reports
- ARTICUL/EZE 2531-52-000TEMPLATE226 reports
- ARTICUL/EZE 1365-22-000Prosthesis, hip, semi-constrained, metal/polymer, cemented220 reports
- ARTICUL/EZE 2530-92-000TEMPLATE203 reports
- ARTICUL/EZE 1365-12-000Prosthesis, hip, semi-constrained, metal/polymer, cemented202 reports
- ARTICUL/EZE 1365-13-000Prosthesis, hip, semi-constrained, metal/polymer, cemented1 death147 reports
- ARTICUL/EZE 2531-53-000TEMPLATE136 reports
- ARTICUL/EZE 2530-93-000TEMPLATE129 reports
- ARTICUL/EZE 1365-23-000Prosthesis, hip, semi-constrained, metal/polymer, cemented124 reports
- ARTICUL/EZE 2531-50-000TEMPLATE87 reports
- ARTICUL/EZE 1365-24-000Prosthesis, hip, semi-constrained, metal/polymer, cemented67 reports
- ARTICUL/EZE 2530-81-000TEMPLATE57 reports
- ARTICUL/EZE 2530-82-000TEMPLATE52 reports
- ARTICUL/EZE 2531-54-000TEMPLATE52 reports
- ARTICUL/EZE 2530-94-000TEMPLATE43 reports
- ARTICUL/EZE 1365-14-000Prosthesis, hip, semi-constrained, metal/polymer, cemented40 reports
- ARTICUL/EZE 2530-83-000TEMPLATE39 reports
- ARTICUL/EZE 2530-84-000TEMPLATE28 reports
- ARTICUL/EZE 1365-15-000Prosthesis, hip, semi-constrained, metal/polymer, cemented21 reports
- ARTICUL/EZE 1365-25-000Prosthesis, hip, semi-constrained, metal/polymer, cemented9 reports
- ARTICUL/EZE 2530-69-000TEMPLATE8 reports
- ARTICUL/EZE 2530-70-000TEMPLATE4 reports
- ARTICUL/EZE 2217-50-066TRAY, SURGICAL, INSTRUMENT1 report
Recent ARTICUL/EZE adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 22, 2026Scratched Material; Illegible Information
It was reported that a 32 Art/eze head trial has scratching in it. Located in loaner hip instrument sets
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50857500 ↗InjurySep 21, 2026Device Dislodged or Dislocated
Patient problems: Joint Dislocation
MAUDE report 50847994 ↗MalfunctionSep 18, 2026Scratched Material; Illegible Information
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50824457 ↗MalfunctionSep 18, 2026Scratched Material; Illegible Information
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50824216 ↗MalfunctionSep 18, 2026Scratched Material; Illegible Information
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50824200 ↗MalfunctionSep 18, 2026Scratched Material; Illegible Information
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50824154 ↗MalfunctionSep 18, 2026Scratched Material; Illegible Information
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50824039 ↗MalfunctionSep 18, 2026Scratched Material; Illegible Information
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50824000 ↗MalfunctionSep 18, 2026Scratched Material; Illegible Information
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50823950 ↗MalfunctionSep 18, 2026Scratched Material; Illegible Information
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50823852 ↗MalfunctionSep 18, 2026Scratched Material; Illegible Information
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50823811 ↗MalfunctionSep 18, 2026Scratched Material; Illegible Information
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50823780 ↗InjurySep 18, 2026Device Dislodged or Dislocated
It was reported that the poly exchange due to anterior dislocation.Affected side: Right Hip.
Patient problems: Joint Dislocation
MAUDE report 50820579 ↗InjurySep 18, 2026Device Dislodged or Dislocated
It was reported that recurrent left hip dislocations.DOI: (b)(6) 2026.DOR: (b)(6) 2026.Affected Side: Unknown.
Patient problems: Joint Dislocation
MAUDE report 50817295 ↗InjurySep 14, 2026Adverse Event Without Identified Device or Use Problem
It was reported that Patient was revised for infected bipolar hip. Head was exchanged.DOI: Unknown.DOR:(b)(6) 2026.Affected Side: Unknown Hip.
Patient problems: Unspecified Infection
MAUDE report 50756070 ↗
Other Depuy (Ireland) products
All Depuy (Ireland) devices →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.
How reports and recalls are matched · Editorial policy · Report an error on this page