DJO SURGICALRecalls & reported problems across all models
Djo, LLC · 42 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 98
- Deaths reported
- 0
- Injuries reported
- 77
- Recalls
- 0
We found 42 models of DJO SURGICAL by Djo, LLC in the FDA's device registry (GUDID). Together they are named in 98 adverse event reports in the FDA's MAUDE database, received between Jun 21, 2016 and Jun 22, 2026 — classified as 77 injuries, 21 malfunctions.
The most frequently reported specific device problem is “Break” (12 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 DJO SURGICAL problems
Device problems
- Adverse Event Without Identified Device or Use Problem31
- Appropriate Device Problem Term/Code Not Available25
- Break12
- Device Dislodged or Dislocated7
- Insufficient Device Problem Information5
- Dull, Blunt4
- Loose or Intermittent Connection3
- Naturally Worn3
Patient problems
- Unspecified Infection34
- Insufficient Information18
- No Known Impact Or Consequence To Patient10
- Joint Laxity7
- No Code Available6
- No Clinical Signs, Symptoms or Conditions4
- No Information4
- Discomfort3
DJO SURGICAL models
42 models, most reported first. Each model has its own page with its reports, recalls and device details.
- DJO SURGICAL 931-36-756Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented13 reports
- DJO SURGICAL 931-36-760Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented13 reports
- DJO SURGICAL 932-36-756Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented13 reports
- DJO SURGICAL 500-04-146Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented5 reports
- DJO SURGICAL 932-36-760PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED4 reports
- DJO SURGICAL 803-00-015Orthopedic manual surgical instrument3 reports
- DJO SURGICAL 804-06-012REAMER3 reports
- DJO SURGICAL 804-06-013REAMER3 reports
- DJO SURGICAL 412-01-054Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented2 reports
- DJO SURGICAL 438-01-003Prosthesis, hip, constrained, cemented or uncemented, metal/polymer2 reports
- DJO SURGICAL 932-40-760PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 reports
- DJO SURGICAL 233-08-110PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER2 reports
- DJO SURGICAL 801-01-650Guide, surgical, instrument2 reports
- DJO SURGICAL 800-05-024Orthopedic manual surgical instrument2 reports
- DJO SURGICAL 800-05-025IMPACTOR2 reports
- DJO SURGICAL 400-02-044Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- DJO SURGICAL 402-28-000Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- DJO SURGICAL 402-32-005Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- DJO SURGICAL 402-32-010Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- DJO SURGICAL 412-01-044Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented1 report
- DJO SURGICAL 412-01-056Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented1 report
- DJO SURGICAL 412-02-041Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented1 report
- DJO SURGICAL 431-22-203PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- DJO SURGICAL 431-28-206PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- DJO SURGICAL 433-32-207Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- DJO SURGICAL 434-28-208Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- DJO SURGICAL 803-21-026Guide, surgical, instrument1 report
- DJO SURGICAL 931-36-764PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- DJO SURGICAL 931-40-760PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- DJO SURGICAL 933-36-764PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- DJO SURGICAL 803-05-229BIT, DRILL1 report
- DJO SURGICAL 803-05-230BIT, DRILL1 report
- DJO SURGICAL 233-08-105PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- DJO SURGICAL 233-08-106PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- DJO SURGICAL 233-08-108PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- DJO SURGICAL 233-09-103PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- DJO SURGICAL 233-09-105PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- DJO SURGICAL 233-09-107PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- DJO SURGICAL 800-01-017HAMMER, SURGICAL1 report
- DJO SURGICAL 804-02-035EXTRACTOR1 report
- DJO SURGICAL 804-03-009Guide, surgical, instrument1 report
- DJO SURGICAL S-200698Guide, surgical, instrument1 report
Recent DJO SURGICAL adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryJun 22, 2026Patient Device Interaction Problem
REVISION SURGERY - DUE TO HAS PAIN ASSOCIATED WITH EXTERNAL ROTATION AND ABDUCTION OF THE HIP.
Patient problems: Implant Pain
MAUDE report 25586570 ↗InjuryApr 30, 2026Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO THE PATIENT HAD SEVERE FALL AND CEMENTED ACETABULUM SPUN OUT AFTER PRIMARY LEFT TOTAL HIP.
Patient problems: Fall
MAUDE report 25049891 ↗InjuryApr 24, 2026Adverse Event Without Identified Device or Use Problem
REVISION SURGERY: DUE TO SPACER REMOVAL. REIMPLANTATION; UNKNOWN REASON.
Patient problems: Insufficient Information
MAUDE report 24990888 ↗InjuryApr 23, 2026Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO UNKNOWN REASON.
Patient problems: Insufficient Information
MAUDE report 24974722 ↗InjuryMar 19, 2026Adverse Event Without Identified Device or Use Problem
InjuryOct 16, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT HETEROTOPIC OSSIFICATION OCCURRED. A NEW LINER AND HEAD WERE IMPLANTED. THE PART NUMBER FOR THE HEAD WAS UNRECOGNIZABLE, SO IT COULD NOT BE IDENTIFIED.
Patient problems: Extraskeletal ossification
MAUDE report 23319299 ↗InjuryJul 29, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryApr 17, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryJan 14, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryDec 6, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY REQUIRED FOR INFECTION.
Patient problems: Unspecified Infection
MAUDE report 20861254 ↗InjuryNov 1, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryJan 18, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryDec 28, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryNov 27, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO WEAR AND TEAR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18213144 ↗InjuryAug 18, 2023Unstable; Adverse Event Without Identified Device or Use Problem; Unstable; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO INSTABILITY AND INFECTION.
Patient problems: Joint Laxity; Unspecified Infection
MAUDE report 17578666 ↗
Other Djo, LLC products
All Djo, LLC 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.
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