DJO SURGICAL 520-01-250Recalls & reported problems
Encore Medical, L.P. · Turon Pegged Glenoid Implant, Size 50 · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Quick summary
This DJO Turon glenoid implant is a cemented shoulder replacement part. Reports mostly describe revision surgery for worn or loose implants, with some mentioning infection, loosened joints, pain and bone loss. There are 26 reports that name its identifier, with no deaths and 26 injuries. 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
- 26
- Deaths reported
- 0
- Injuries reported
- 26
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 26 adverse event reports that list this exact device (DI 00888912024976), received between Dec 16, 2015 and Jan 20, 2026 — classified as 26 injuries.
The most frequently reported specific device problem is “Loose or Intermittent Connection” (2 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, 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 Problem13
- Appropriate Device Problem Term/Code Not Available9
- Loose or Intermittent Connection2
- Insufficient Device Problem Information1
- Loosening of Implant Not Related to Bone-Ingrowth1
- Naturally Worn1
- Patient-Device Incompatibility1
Patient problems
- Joint Laxity9
- Unspecified Infection6
- Failure of Implant4
- Insufficient Information4
- No Code Available3
- Implant Pain2
Recent adverse event reports
The 25 most recent of 26 reports, in the reporter's own words as published by the FDA.
InjuryJan 20, 2026Naturally Worn
InjuryNov 26, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryOct 17, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryMay 24, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryFeb 25, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryJan 16, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO LOOSE IMPLANT/PAIN.
Patient problems: Implant Pain; Joint Laxity
MAUDE report 21175489 ↗InjuryOct 24, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryOct 22, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjurySep 6, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryMay 19, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO PAIN AND LOOSENING.
Patient problems: Implant Pain; Joint Laxity
MAUDE report 16969437 ↗InjuryJan 26, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjurySep 8, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryMay 4, 2022Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - FAILED ROTATOR CUFF. CONVERSION FROM TOTAL SHOULDER ARTHROPLASTY TO REVERSE.
Patient problems: Insufficient Information
MAUDE report 14273747 ↗InjuryAug 18, 2021Adverse Event Without Identified Device or Use Problem
InjuryJun 30, 2021Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - PATIENT NEEDED TO BE REVISED TO A REVERSE.
Patient problems: Insufficient Information
MAUDE report 12093302 ↗InjuryJun 28, 2021Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - UNKNOWN REASON, POSSIBLY FAILED ROTATOR CUFF BUT NOT 100% SURE. CONVERTED TO REVERSE.
Patient problems: Insufficient Information
MAUDE report 12080871 ↗InjuryJun 2, 2021Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - THE SURGEON DID NOT SPECIFY CAUSE.
Patient problems: Insufficient Information
MAUDE report 11919111 ↗InjuryDec 17, 2019Loose or Intermittent Connection; Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - TURON GLENOID IMPLANT LOOSENING DUE TO INFECTION.
Patient problems: Unspecified Infection
MAUDE report 9481854 ↗InjuryAug 1, 2019Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - PATIENT PRESENTED TO SURGEON'S OFFICE WITH SYMPTOMS OF INFECTION. SURGEON OPTED TO IRRIGATION & DRAINAGE AND REMOVE ALL IMPLANTS. CEMENTED SPACER WAS IMPLANTED TEMPORARILY TO COMBAT INFECTIONS.
Patient problems: Unspecified Infection
MAUDE report 8852928 ↗InjuryJul 3, 2019Appropriate Device Problem Term/Code Not Available; Loosening of Implant Not Related to Bone-Ingrowth
REVISION SURGERY - DUE TO GLENOID LOOSENING.
Patient problems: Failure of Implant
MAUDE report 8759991 ↗InjuryFeb 21, 2018Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - DUE TO FAILED ROTATOR CUFF.
Patient problems: No Code Available
MAUDE report 7286788 ↗InjuryNov 10, 2017Loose or Intermittent Connection
REVISION SURGERY - DUE TO THE PATIENT HAVING A LOOSE GLENOID COMPONENT.
Patient problems: No Code Available
MAUDE report 7018660 ↗InjuryAug 16, 2017Insufficient Device Problem Information
REVISION SURGERY - ALL PREVIOUS IMPLANTS WERE REMOVED AND CONVERTED TO A REVERSE DUE TO ROTATOR CUFF TEAR.
Patient problems: No Code Available
MAUDE report 6797202 ↗InjuryMar 3, 2017Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO THE PATIENT HAVING AN INFECTION.
Patient problems: Unspecified Infection
MAUDE report 6378620 ↗InjuryFeb 3, 2017Patient-Device Incompatibility
REVISION SURGERY - DUE TO THE PATIENT TEARING THEIR ROTATOR CUFF, CAUSING THE TURON IMPLANTS TO FAIL.
Patient problems: Failure of Implant
MAUDE report 6301259 ↗
Other Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented devices
- DJO SURGICAL 508-32-204Encore Medical, L.P. · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 recall544 reports
- Comprehensive Reverse Shoulder 010000589Biomet Orthopedics, LLC · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 recall142 reports
- DELTA XTEND 130738203Depuy (Ireland) · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED175 reports
- DJO SURGICAL 509-00-432Encore Medical, L.P. · Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented1 recall117 reports
- Alliance® SBGL3007Zimmer, Inc. · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED162 reports
- DELTA XTEND 130760138Depuy (Ireland) · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED146 reports
- DELTA XTEND 130790030Depuy (Ireland) · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED132 reports
- DJO SURGICAL 509-00-436Encore Medical, L.P. · Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented124 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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