DJO SURGICAL 508-32-101Recalls & reported problems
Encore Medical, L.P. · GLENOID, HEAD W/RETAINING SCREW, RSP, 32MM/NEUTRAL · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Quick summary
This DJO Surgical reverse shoulder glenoid has 432 adverse event reports, with 432 injuries and no deaths. The reports mostly describe parts coming loose, shoulder instability and joint dislocation, and several describe revision surgery, some due to infection. 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
- 433
- Deaths reported
- 0
- Injuries reported
- 433
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 433 adverse event reports that list this exact device (DI 00888912024730), received between Sep 16, 2015 and Sep 8, 2026 — classified as 433 injuries.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (153 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 Problem171
- Device Dislodged or Dislocated153
- Appropriate Device Problem Term/Code Not Available86
- Unstable54
- Insufficient Device Problem Information15
- Break9
- Fracture4
- Loose or Intermittent Connection4
Patient problems
- Joint Dislocation176
- No Code Available75
- Insufficient Information48
- Unspecified Infection32
- Joint Laxity25
- No Known Impact Or Consequence To Patient25
- Failure of Implant23
- Fall13
Recent adverse event reports
The 25 most recent of 433 reports, in the reporter's own words as published by the FDA.
InjurySep 8, 2026Unstable
Patient problems: Joint Laxity
MAUDE report 50678683 ↗InjuryJun 29, 2026Unstable
REVISION SURGERY - DUE TO THE PATIENT BECAME UNSTABLE AND NEEDED TO HAVE A LARGER GLENOSPHERE.
Patient problems: Joint Laxity
MAUDE report 25660425 ↗InjuryJun 29, 2026Adverse Event Without Identified Device or Use Problem
InjuryJun 25, 2026Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO THE PATIENT HAD AN INFECTION AND NEEDED TO HAVE NEW IMPLANTS.
Patient problems: Unspecified Infection
MAUDE report 25628147 ↗InjuryMay 26, 2026Device Dislodged or Dislocated
REVISION SURGERY - DUE TO THE GLENOSHPERE BECAME DETACHED FROM THE BASEPLATE, LIKELY DUE TO PERIPHERAL SCREWS NOT BEING FULLY SEATED.
Patient problems: Joint Laxity
MAUDE report 25294012 ↗InjuryMay 26, 2026Device Dislodged or Dislocated
REVISION SURGERY DUE TO PATIENT HAD DISLOCATED. GLENOSPHERE AND LINER WERE REMOVED AND REPLACED WITH A MORE STABLE CONSTRUCT.
Patient problems: Joint Dislocation
MAUDE report 25276476 ↗InjuryMay 22, 2026Device Dislodged or Dislocated
InjuryMay 21, 2026Insufficient Device Problem Information
REVISION SURGERY - THE SURGEON DECIDED TO REPOSITION THE BASE PLATE AND DOWNSIZE THE GLENOID HEAD TO A 32-4, UNKNOWN REASON.
Patient problems: Insufficient Information
MAUDE report 25250362 ↗InjuryMay 14, 2026Unstable
REVISION SURGERY DUE TO THE PATIENTS SHOULDER JOINT WAS MORE MOBILE THAN THE SURGEON LIKED, LOOSE.
Patient problems: Joint Laxity
MAUDE report 25179174 ↗InjuryMay 5, 2026Insufficient Device Problem Information
REVISION SURGERY - SCAPULAR NOTCHING DUE TO UNKNOWN REASON.
Patient problems: Insufficient Information
MAUDE report 25088845 ↗InjuryApr 8, 2026Adverse Event Without Identified Device or Use Problem
InjuryApr 6, 2026Device Dislodged or Dislocated
InjuryMar 25, 2026Adverse Event Without Identified Device or Use Problem
InjuryMar 17, 2026Adverse Event Without Identified Device or Use Problem
CHRONIC DISLOCATION+ FRACTURE. 70 YR OLD FEMALE.
Patient problems: Joint Dislocation
MAUDE report 24622297 ↗InjuryMar 16, 2026Adverse Event Without Identified Device or Use Problem
THE PATIENT DISLOCATED ONCE. AND THEN DISLOCATED AGAIN AFTER A CLOSED REDUCTION. DR (B)(6) WENT TO A LARGER GLENOSPHERE AND THICKER INSERT TO CREATE MORE STABILITY.
Patient problems: Joint Dislocation
MAUDE report 24609414 ↗InjuryMar 11, 2026Device Dislodged or Dislocated
InjuryMar 5, 2026Adverse Event Without Identified Device or Use Problem
InjuryJan 30, 2026Unstable; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO PAIN AND INSTABILITY
Patient problems: Joint Laxity; Pain
MAUDE report 24228992 ↗InjuryJan 26, 2026Device Dislodged or Dislocated
InjuryJan 16, 2026Device Dislodged or Dislocated
InjuryJan 16, 2026Device Dislodged or Dislocated
InjuryJan 14, 2026Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO INFECTION AND PAIN.
Patient problems: Pain; Unspecified Infection
MAUDE report 24077045 ↗InjuryJan 9, 2026Device Dislodged or Dislocated
InjuryJan 7, 2026Adverse Event Without Identified Device or Use Problem
InjuryJan 6, 2026Adverse Event Without Identified Device or Use Problem
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 508-32-103Encore Medical, L.P. · shoulder prosthesis, reverse configuration421 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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