DJO SURGICAL 508-32-103Recalls & reported problems
Encore Medical, L.P. · GLENOID, HEAD W/RETAINING SCREW, RSP, 32MM/-4MM · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Quick summary
This DJO Surgical reverse shoulder glenoid implant has 421 reports, including 418 injuries and no deaths. Common reports describe the implant dislodging or loosening, with the shoulder dislocating or feeling unstable, and some patients needed revision surgery. No recalls name this device.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 421
- Deaths reported
- 0
- Injuries reported
- 418
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 421 adverse event reports that list this exact device (DI 00888912024747), received between Sep 15, 2015 and Sep 28, 2026 — classified as 418 injuries, 3 malfunctions.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (131 reports).
5 other recalls cover devices cleared under the same FDA submission (K051075); they may or may not involve this specific model.
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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem190
- Device Dislodged or Dislocated131
- Appropriate Device Problem Term/Code Not Available77
- Unstable56
- Fracture8
- Loosening of Implant Not Related to Bone-Ingrowth8
- Loose or Intermittent Connection7
- Insufficient Device Problem Information4
Patient problems
- Joint Dislocation180
- Joint Laxity51
- No Code Available45
- Insufficient Information30
- No Known Impact Or Consequence To Patient28
- Failure of Implant25
- Pain23
- Unspecified Infection23
Recent adverse event reports
The 25 most recent of 421 reports, in the reporter's own words as published by the FDA.
InjurySep 28, 2026Patient Device Interaction Problem
Patient problems: Pain
MAUDE report 50926100 ↗InjurySep 16, 2026Adverse Event Without Identified Device or Use Problem
Patient problems: Joint Impingement
MAUDE report 50796862 ↗InjurySep 9, 2026Unstable
Patient problems: Joint Laxity
MAUDE report 50681098 ↗InjuryAug 31, 2026Device Dislodged or Dislocated
InjuryJul 8, 2026Loosening of Implant Not Related to Bone-Ingrowth
InjuryJul 6, 2026Device Dislodged or Dislocated
InjuryJun 23, 2026Loosening of Implant Not Related to Bone-Ingrowth
REVISION SURGERY - DUE TO LOOSE GLENOID IMPLANT.
Patient problems: Joint Laxity
MAUDE report 25601920 ↗InjuryJun 15, 2026Unstable; Device Dislodged or Dislocated
REVISION SURGERY DUE TO DISLOCATION / INSTABILITY.
Patient problems: Joint Laxity
MAUDE report 25512069 ↗InjuryJun 11, 2026Device Dislodged or Dislocated
InjuryJun 9, 2026Unstable
PATIENT HAD A LOOSE BASEPLATE AFTER A REVISION ALREADY, SURGEON TOOK OUT BASEPLATE, GLENOSPHERE, AND POLY AND CONVERTED THE PATIENT TO A HEMI.
Patient problems: Joint Laxity
MAUDE report 25445756 ↗InjuryJun 1, 2026Unstable; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO PAIN AND INSTABILITY.
Patient problems: Joint Laxity; Pain
MAUDE report 25355613 ↗InjuryMay 29, 2026Adverse Event Without Identified Device or Use Problem
InjuryApr 24, 2026Device Dislodged or Dislocated
InjuryApr 23, 2026Unstable
REVISION SURGERY- DUE TO INSTABILITY UPSIZED SPHERE FROM 32 TO A 36.
Patient problems: Joint Laxity
MAUDE report 24974724 ↗InjuryApr 20, 2026Unstable
REVISION SURGERY - TO TREAT INSTABILITY AND POSSIBLE INFECTION.
Patient problems: Joint Laxity; Unspecified Infection
MAUDE report 24933743 ↗InjuryApr 13, 2026Adverse Event Without Identified Device or Use Problem
PATIENT DISLOCATED SO NEEDED TO ADD MORE TENSION BY USING A BIGGER SPHERE.
Patient problems: Joint Laxity
MAUDE report 24865476 ↗InjuryApr 9, 2026Adverse Event Without Identified Device or Use Problem
InjuryApr 8, 2026Unstable; Adverse Event Without Identified Device or Use Problem
InjuryApr 1, 2026Unstable; Adverse Event Without Identified Device or Use Problem
PATIENT WAS CHRONIC DISLOCATOR. WE WENT TO 36 GLENOSHERE, 12 MM SPACER AND PLUS 4 POLY.
Patient problems: Joint Dislocation
MAUDE report 24754236 ↗InjuryMar 25, 2026Adverse Event Without Identified Device or Use Problem
InjuryMar 25, 2026Adverse Event Without Identified Device or Use Problem
THE PATIENT WAS UNHAPPY WITH HIS CURRENT IMPLANTS/ WANTED A REVISION. MALE 77YRS.
Patient problems: Implant Pain
MAUDE report 24693906 ↗InjuryMar 25, 2026Unstable; Adverse Event Without Identified Device or Use Problem
PATIENT PRESENTED LOOSENING OF GLENOID COMPONENT AND BROKEN CENTRAL SCREW. SURGEON OPTED TO REPLACE GLENOID WITH CUSTOM GLENOID IMPLANT, WHICH FAILED INTRAOPERATIVE. SO SURGEON OPTED FOR A HERU-ARTHOPLASTY WITH ENOVIS STEM (CONVERTED). 56 YR OLD FEMALE.
Patient problems: Joint Laxity
MAUDE report 24693904 ↗InjuryMar 25, 2026Mechanical Problem
PT PRESENTED WITH SOME IMPINGEMENT, DR. INCREASED THE SIZE OF GLENOSPHERES AND POLY TO PREVENT THIS. HAPPY WITH THE OUTCOME OF THE HEAD/LINER EXCHANGE. FEMALE.
Patient problems: Joint Impingement
MAUDE report 24683773 ↗InjuryMar 16, 2026Unstable; Adverse Event Without Identified Device or Use Problem
PATIENT HAD INSTABILITY AND THEIR SHOULDER WAS DISLOCATING. SURGEON WANTED TO SWITCH OUT GLENOSPHERE AND POLY FOR MORE STABILITY.
Patient problems: Joint Dislocation; Joint Laxity
MAUDE report 24610019 ↗InjuryMar 12, 2026Unstable; Device Dislodged or Dislocated
REVISION SURGERY - DUE TO SUBLUXATION
Patient problems: Joint Dislocation; Joint Laxity
MAUDE report 24587608 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K051075. One submission often covers many models, so check the product and lot details in each record.
- Z-1460-2026 · Jan 15, 2026 · Open, ClassifiedBrand Name: Reverse Shoulder Prosthesis (RSP) Product Name: RSP STANDARD HUMERAL SOCKET INSERT, 36MM, HXe-plus Model/Catalog Number: 509-00-036
- Z-0625-2024 · Oct 5, 2023 · CompletedReverse Shoulder System e+, REF 509-01-032, RSP Humeral Socket Insert, Sz. 32mm, Semi-Constrained, Sterile H2o2, CE 2797
- Z-0282-2024 · Sep 25, 2023 · Open, ClassifiedRSP Humeral Socket Insert Size 36mm Semi-Constrained +4 mm, REF: 509-01-436, orthopedic shoulder implant component.
- Z-2606-2023 · Aug 4, 2023 · Open, ClassifiedDJO Surgical: Reverse Shoulder System (RSP) Semi Humeral Socket Insert, 32mm, REF: 508-01-032; Baseplate, Glenoid HA-Coat, RSP, 6.5mm X 30mm, REF: 508-32-104; Reverse Shoulder Syst
- Z-2739-2011 · Apr 18, 2011 · TerminatedReverse Shoulder Prosthesis System RSP Humeral Socket Shell DJO 9800 Metric Blvd. Austin, TX 78758 STERILE R Model numbers: 508-00-000 and 508-00-008. The Reverse Shoulder Prost
Other shoulder prosthesis, reverse configuration devices
- DJO SURGICAL 508-36-101Encore Medical, L.P. · shoulder prosthesis, reverse configuration508 reports
- DJO SURGICAL 508-32-101Encore Medical, L.P. · shoulder prosthesis, reverse configuration433 reports
- DJO SURGICAL 509-00-036Encore Medical, L.P. · shoulder prosthesis, reverse configuration1 recall259 reports
- DJO SURGICAL 508-32-104Encore Medical, L.P. · shoulder prosthesis, reverse configuration1 recall203 reports
- DJO SURGICAL 509-00-032Encore Medical, L.P. · shoulder prosthesis, reverse configuration233 reports
- DELTA XTEND 130760000Depuy (Ireland) · shoulder prosthesis, reverse configuration223 reports
- DJO SURGICAL 508-00-032Encore Medical, L.P. · shoulder prosthesis, reverse configuration122 reports
- DJO SURGICAL 509-01-436Encore Medical, L.P. · shoulder prosthesis, reverse configuration1 recall62 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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