DJO SURGICAL 520-01-242Recalls & reported problems
Encore Medical, L.P. · Turon Pegged Glenoid Implant, Size 42 · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Quick summary
This DJO Turon shoulder implant replaces the socket part of the shoulder joint. Reports mostly describe loosening, wear and instability that led to follow-up surgery to revise or replace the implant. There are 26 reports naming 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 00888912024952), received between Sep 11, 2015 and Mar 18, 2026 — classified as 26 injuries.
The most frequently reported specific device problem is “Loose or Intermittent Connection” (4 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 Problem12
- Appropriate Device Problem Term/Code Not Available4
- Loose or Intermittent Connection4
- Insufficient Device Problem Information2
- Torn Material2
- Device Operates Differently Than Expected1
- Loosening of Implant Not Related to Bone-Ingrowth1
- Material Split, Cut or Torn1
Patient problems
- Failure of Implant6
- Joint Laxity5
- Insufficient Information4
- No Code Available4
- Unspecified Infection2
- Discomfort1
- Fall1
- Implant Pain1
Recent adverse event reports
The 25 most recent of 26 reports, in the reporter's own words as published by the FDA.
InjuryMar 18, 2026Adverse Event Without Identified Device or Use Problem
FAILED ANATOMIC SHOULDER REPLACEMENT WITH ANTERIOR WEAR OF GLENOID COMPONENT.
Patient problems: Failure of Implant; Insufficient Information
MAUDE report 24631503 ↗InjuryJul 1, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryApr 29, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryNov 11, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryJul 10, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
"REVISION" SURGERY - DUE TO IMPLANT FAILURE.
Patient problems: Failure of Implant
MAUDE report 19717060 ↗InjuryOct 19, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - PATIENT HAD A ROTATOR CUFF INJURY AND NEEDED TO BE CONVERTED TO REVERSE SHOULDER.
Patient problems: Joint Laxity
MAUDE report 17971376 ↗InjurySep 19, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - SOFT TISSUE ISSUE.
Patient problems: Insufficient Information
MAUDE report 17778211 ↗InjurySep 5, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO POLY WEAR AND INSTABILITY.
Patient problems: Joint Laxity
MAUDE report 17687360 ↗InjuryAug 10, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO FAILED GLENOID.
Patient problems: Failure of Implant
MAUDE report 17504810 ↗InjuryDec 13, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO GLENOID BECAME LOOSE.
Patient problems: Joint Laxity
MAUDE report 15970235 ↗InjuryNov 23, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryOct 7, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - CUFF TEAR AND GLENOID WEAR.
Patient problems: Muscle/Tendon Damage
MAUDE report 15564012 ↗InjurySep 3, 2021Loosening of Implant Not Related to Bone-Ingrowth
REVISION SURGERY - DUE TO GLENOID LOOSENING.
Patient problems: Failure of Implant
MAUDE report 12421734 ↗InjuryAug 19, 2021Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - PATIENT SUFFERED A BAD FALL AND SUBSEQUENT CUFF ARTHROPATHY, CONVERTED TOTAL SHOULDER TO REVERSE.
Patient problems: Fall
MAUDE report 12345116 ↗InjuryApr 1, 2021Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - THE PATIENT HAD A TURON PRIMARY STEM AND GLENOID COMPONENT IMPLANTED THAT WAS UNSTABLE. SURGEON REMOVED ALL COMPONENTS AND REVISED WITH A REVERSE SHOULDER.
Patient problems: Insufficient Information
MAUDE report 11605226 ↗InjuryDec 4, 2020Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - DUE TO UNKNOWN REASON.
Patient problems: Insufficient Information
MAUDE report 10949850 ↗InjurySep 24, 2020Naturally Worn
REVISION SURGERY - PATIENT HAD PAIN AND LIMITED MOVEMENT. CT SCAN AND X-RAY INDICATED WEAR AND JOINT LOSS.
Patient problems: Limited Mobility Of The Implanted Joint; Pain
MAUDE report 10580159 ↗InjuryAug 3, 2020Loose or Intermittent Connection; Material Split, Cut or Torn
REVISION SURGERY - LOOSE GLENOID AND TORN CUFF.
Patient problems: Failure of Implant
MAUDE report 10355746 ↗InjuryMay 9, 2019Loose or Intermittent Connection
REVISION SURGERY - DUE TO THE GLENOID BEGINNING TO LOOSEN.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8595360 ↗InjuryDec 6, 2017Loose or Intermittent Connection
REVISION SURGERY - DUE TO THE GLENOID COMPONENTS COMING LOOSE OVER TIME. THE PATIENT HAD A TOTAL SHOULDER ARTHROPLASTY (TSA) PROCEDURE IN 2012. THE SURGEON REMOVED THE ORIGINAL COMPONENTS AND CONVERTED TO A REVERSE SHOULDER PROSTHESIS (RSP).
Patient problems: Failure of Implant; No Code Available
MAUDE report 7088777 ↗InjuryDec 4, 2017Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - IT WAS REPORTED IN THE COMPLAINT AS THE PATIENT'S CUFF WAS "SHOT", SO THE SURGEON CONVERTED IT TO A REVERSE.
Patient problems: No Code Available
MAUDE report 7079479 ↗InjurySep 15, 2017Torn Material
REVISION SURGERY - DUE TO PATIENT TEARING HER ROTATOR CUFF. THE SURGEON DID A REVERSE SHOULDER.
Patient problems: No Code Available
MAUDE report 6869199 ↗InjuryAug 8, 2017Device Operates Differently Than Expected; Torn Material
REVISION SURGERY - DUE TO FAILED TOTAL SHOULDER WITH CUFF TEAR WHICH REQUIRED A REVERSE TO BE PUT IN.
Patient problems: No Code Available
MAUDE report 6774626 ↗InjuryMay 31, 2017Insufficient Device Problem Information
REVISION SURGERY - DUE TO THE PATIENT HAVING SUFFERED A TRAUMA TO THEIR SHOULDER AND HAVING AN IRREPARABLE ROTATOR CUFF THAT NEEDED TO BE REVISED.
Patient problems: Injury
MAUDE report 6603385 ↗InjuryFeb 16, 2016Insufficient Device Problem Information
REVISION SURGERY - DUE TO THE PATIENT HAVING AN INFECTION.
Patient problems: Unspecified Infection
MAUDE report 5439379 ↗
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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