DJO SURGICAL 520-01-254Recalls & reported problems
Encore Medical, L.P. · Turon Pegged Glenoid Implant, Size 54 · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 9
- Deaths reported
- 0
- Injuries reported
- 9
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 00888912145107), received between Dec 20, 2017 and Jul 8, 2025 — classified as 9 injuries.
The most frequently reported specific device problem is “Loose or Intermittent Connection” (3 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 Problem4
- Appropriate Device Problem Term/Code Not Available3
- Loose or Intermittent Connection3
- Contamination1
Patient problems
- Joint Laxity3
- Failure of Implant2
- Implant Pain1
- Insufficient Information1
- Joint Dislocation1
- No Code Available1
- No Information1
- Unspecified Infection1
Recent adverse event reports
The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.
InjuryJul 8, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY: DUE TO DISLOCATION AND WEAR.
Patient problems: Joint Dislocation
MAUDE report 22447447 ↗InjuryJan 27, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO LOOSENING AND POLY WEAR.
Patient problems: Joint Laxity
MAUDE report 21248938 ↗InjurySep 19, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO INSTABILITY AND PAIN.
Patient problems: Implant Pain; Joint Laxity
MAUDE report 17778214 ↗InjuryJan 12, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryJul 12, 2021Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - THE PATIENT NEEDED TO BE CONVERTED TO A REVERSE BECAUSE OF A FAILED ROTATOR CUFF.
Patient problems: Failure of Implant
MAUDE report 12153751 ↗InjuryJan 8, 2021Loose or Intermittent Connection; Appropriate Device Problem Term/Code Not Available
SECOND REVISION SURGERY - REMOVED NECK, HEAD, AND GLENOID DUE TO LOOSE GLENOID.
Patient problems: Insufficient Information
MAUDE report 11142659 ↗InjuryJul 8, 2020Loose or Intermittent Connection; Appropriate Device Problem Term/Code Not Available
InjuryMar 1, 2018Loose or Intermittent Connection
REVISION SURGERY - DUE TO THE PATIENT HAVING GLENOID LOOSENING.
Patient problems: No Information
MAUDE report 7307899 ↗InjuryDec 20, 2017Contamination
REVISION SURGERY - DUE TO THE PATIENT HAVING AN INFECTED SHOULDER. THE SURGEON REMOVED THE COMPONENTS AND PLACED AN ANTIBIOTIC SPACER.
Patient problems: No Code Available; Unspecified Infection
MAUDE report 7135702 ↗
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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