ENDURANCERecalls & reported problems across all models
Depuy Orthopaedics, Inc. · 20 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 46
- Deaths reported
- 1
- Injuries reported
- 17
- Recalls
- 0
We found 20 models of ENDURANCE by Depuy Orthopaedics, Inc. in the FDA's device registry (GUDID). Together they are named in 46 adverse event reports in the FDA's MAUDE database, received between Sep 19, 2017 and Aug 31, 2026 — classified as 1 death, 17 injuries, 28 malfunctions.
The most frequently reported specific device problem is “Break” (9 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 ENDURANCE problems
Device problems
- Adverse Event Without Identified Device or Use Problem9
- Break9
- Device-Device Incompatibility8
- Failure to Cut5
- Loss of or Failure to Bond5
- Material Deformation4
- Appropriate Device Problem Term/Code Not Available1
- Component Missing1
Patient problems
- No Clinical Signs, Symptoms or Conditions19
- No Consequences Or Impact To Patient7
- Pain7
- Unspecified Infection6
- No Code Available5
- Not Applicable3
- Test Result3
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available2
ENDURANCE models
20 models, most reported first. Each model has its own page with its reports, recalls and device details.
- ENDURANCE 2521-00-503ORTHOPEDIC MANUAL SURGICAL INSTRUMENT8 reports
- ENDURANCE 2521-00-502DRIVER, PROSTHESIS6 reports
- ENDURANCE 1521-21-000Prosthesis, hip, semi-constrained, metal/polymer, cemented4 reports
- ENDURANCE 1521-22-000Prosthesis, hip, semi-constrained, metal/polymer, cemented1 death3 reports
- ENDURANCE 2521-01-510BROACH3 reports
- ENDURANCE 2521-03-510BROACH3 reports
- ENDURANCE 1521-27-000Prosthesis, hip, semi-constrained, metal/polymer, cemented2 reports
- ENDURANCE 1521-62-000Prosthesis, hip, semi-constrained, metal/polymer, cemented2 reports
- ENDURANCE 2521-02-510BROACH2 reports
- ENDURANCE 2521-04-510BROACH2 reports
- ENDURANCE 2521-05-510BROACH2 reports
- ENDURANCE 1223-50-000Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- ENDURANCE 1521-23-000Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- ENDURANCE 1521-24-000Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- ENDURANCE 1521-25-000Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- ENDURANCE 1521-61-000Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- ENDURANCE 1521-73-000Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- ENDURANCE 2521-00-508EXTRACTOR1 report
- ENDURANCE 2521-01-501ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- ENDURANCE 2521-23-501ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
Recent ENDURANCE adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryAug 31, 2026Adverse Event Without Identified Device or Use Problem
It was reported that the patient was revised due to Pain.DOI: (b)(6) 2026DOR: (b)(6) 2026Affected side: Right.
Patient problems: Pain
MAUDE report 50524462 ↗MalfunctionMay 4, 2026Material Deformation
IT WAS REPORTED THAT THE DAMAGED TIP OF INSERTER WITH TRAYS WAS BEING STACKED ON IT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25067739 ↗MalfunctionApr 9, 2026Material Deformation
IT WAS REPORTED THAT INSERTER TIP FOR ENDURANCE WAS BENT. STRAIGHT REAMER SHAFT WAS WOBBLING. LPS STEM INSERTER WAS BROKEN. THE 45 DEGREE ANGLE DRILL WAS BROKEN. IT DID NOT HAPPENED IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24829895 ↗MalfunctionMar 12, 2025Break; Break
IT WAS REPORTED THAT THE BROACH HANDLE ATTACHMENT AND TRIAL EXTRACTOR BROKE DURING CLEANING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21588022 ↗MalfunctionDec 4, 2024Break; Break
IT WAS REPORTED THAT PATIENT UNDERWENT HIP SURGERY ON NOVEMBER 20, 2024. DURING THE PROCEDURE A HANDLE BROKE AS THE DOCTOR CLASPED THE TRIAL TO REMOVE IT FROM THE FEMUR. A VICE GRIP WAS USED TO REMOVE THE TRIAL. PROCEDURE WAS COMPLETED SUCCESSFULLY WITH A FIVE MINUTE DELAY.
Patient problems: Insufficient Information
MAUDE report 20843480 ↗MalfunctionOct 15, 2024Break; Break
IT WAS REPORTED THAT THE INSTRUMENT IS BROKEN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20449932 ↗MalfunctionAug 29, 2023Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE SZ 1 REPLACEMENT BROACHES ARRIVED AND WERE A DIFFERENT DESIGN. NECK SEGMENTS WERE TOO LOOSE ON THE NEW BROACHES. UNKNOWN SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17642416 ↗MalfunctionAug 28, 2023Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE SZ 1 REPLACEMENT BROACHES ARRIVED AND WERE A DIFFERENT DESIGN. NECK SEGMENTS WERE TOO LOOSE ON THE NEW BROACHES. UNKNOWN SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17636102 ↗MalfunctionAug 28, 2023Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE SZ 1 REPLACEMENT BROACHES ARRIVED AND WERE A DIFFERENT DESIGN. NECK SEGMENTS WERE TOO LOOSE ON THE NEW BROACHES. UNKNOWN SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17635640 ↗MalfunctionAug 28, 2023Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE SZ 1 REPLACEMENT BROACHES ARRIVED AND WERE A DIFFERENT DESIGN. NECK SEGMENTS WERE TOO LOOSE ON THE NEW BROACHES. UNKNOWN SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17635013 ↗MalfunctionAug 28, 2023Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE SZ 1 REPLACEMENT BROACHES ARRIVED AND WERE A DIFFERENT DESIGN. NECK SEGMENTS WERE TOO LOOSE ON THE NEW BROACHES. UNKNOWN SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17634582 ↗MalfunctionAug 28, 2023Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE SZ 1 REPLACEMENT BROACHES ARRIVED AND WERE A DIFFERENT DESIGN. NECK SEGMENTS WERE TOO LOOSE ON THE NEW BROACHES. UNKNOWN SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17634501 ↗MalfunctionAug 28, 2023Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE SZ 1 REPLACEMENT BROACHES ARRIVED AND WERE A DIFFERENT DESIGN. NECK SEGMENTS WERE TOO LOOSE ON THE NEW BROACHES. UNKNOWN SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17634305 ↗MalfunctionAug 22, 2023Device-Device Incompatibility; Material Deformation; Unintended Movement; Device-Device Incompatibility; Material Deformation; Unintended Movement
IT WAS REPORTED THAT THE SIZE 1 ENDURANCE BROACH HAS BEEN WARPED SO THAT IT IS LOOSE AND UNSTABLE IN THE BROACH HANDLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17595895 ↗InjuryMay 24, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
PATIENT WAS REVISED DUE TO INFECTED HIP. SURGICAL DELAY WAS UNKNOWN. DOI: UNKNOWN. DOR: (B)(6) 2023. AFFECTED SIDE: RIGHT HIP.
Patient problems: Unspecified Infection
MAUDE report 16991409 ↗
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
- DURALOC93 models · 1,262 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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