DJO SURGICAL 521-01-242Recalls & reported problems
Encore Medical, L.P. · TURON PEGGED GLENOID, SZ 42MM, eplus · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 17
- Deaths reported
- 0
- Injuries reported
- 17
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 17 adverse event reports that list this exact device (DI 00888912145367), received between Dec 23, 2015 and Aug 12, 2025 — classified as 17 injuries.
The most frequently reported specific device problem is “Device Operates Differently Than Expected” (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 Problem5
- Device Operates Differently Than Expected4
- Appropriate Device Problem Term/Code Not Available3
- Loose or Intermittent Connection2
- Inadequacy of Device Shape and/or Size1
- Insufficient Device Problem Information1
- Material Deformation1
- Therapeutic or Diagnostic Output Failure1
Patient problems
- No Code Available5
- Implant Pain3
- Joint Laxity3
- Failure of Implant2
- Pain2
- Insufficient Information1
- Laceration(s)1
- Loss of Range of Motion1
Recent adverse event reports
The 17 most recent of 17 reports, in the reporter's own words as published by the FDA.
InjuryAug 12, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryMar 27, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO PAIN AND LOSS OF RANGE OF MOTION.
Patient problems: Implant Pain; Loss of Range of Motion
MAUDE report 21715479 ↗InjuryFeb 4, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryJul 18, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO WEARING / REQUIRED INTERVENTION TO PREVENT IMPAIRMENT/DAMAGE.
Patient problems: Joint Laxity
MAUDE report 17347248 ↗InjuryApr 27, 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 16827797 ↗InjuryJul 13, 2022Therapeutic or Diagnostic Output Failure
REVISION SURGERY: PATIENT COMPLAINED OF PAIN AND WAS DIAGNOSED WITH ROTATOR CUFF TEAR. REVISED TURON ANATOMIC SHOULDER TO A REVERSE SHOULDER LEAVING TURON STEM INTACT AND ADDING CUP ADAPTER TO STEM.
Patient problems: Pain
MAUDE report 15001942 ↗InjuryMar 15, 2022Loose or Intermittent Connection; Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - SUBSCAP FAILURE LEADING TO GLENOID COMPONENT FAILURE, LOOSENING.
Patient problems: Insufficient Information
MAUDE report 13775077 ↗InjuryFeb 9, 2022Appropriate Device Problem Term/Code Not Available
REVISION SURGERY: TOTAL SHOULDER ARTHROPLASTY REVISED TO HEMI/ANTIBIOTIC SPACER DUE TO SEVERE INFECTION.
Patient problems: Unspecified Infection
MAUDE report 13499698 ↗InjuryFeb 8, 2022Appropriate Device Problem Term/Code Not Available
REVISION SURGERY SURGEON REVISED THE PATIENT TO A REVERSE TOTAL SHOULDER DUE TO A FAILED TOTAL SHOULDER.
Patient problems: Failure of Implant
MAUDE report 13479960 ↗InjuryJan 7, 2021Loose or Intermittent Connection; Unstable
REVISION SURGERY - SHOULDER PAIN AFTER PRIMARY SURGERY. GLENOID LOOSENING AND INSTABILITY.
Patient problems: Failure of Implant
MAUDE report 11133564 ↗InjuryFeb 9, 2018Device Operates Differently Than Expected
REVISION SURGERY - DUE TO A FAILED ROTATOR CUFF AND THE SURGEON NEEDING TO CONVERT TO A REVERSE SHOULDER.
Patient problems: No Code Available
MAUDE report 7259379 ↗InjuryFeb 1, 2018Device Operates Differently Than Expected
REVISION SURGERY - DUE TO THE PATIENT HAVING A CUFF FAILURE.
Patient problems: No Code Available
MAUDE report 7233966 ↗InjuryJan 22, 2018Material Deformation
REVISION SURGERY - DUE TO THE PATIENT HAVING ROTATOR CUP DEFICIENCY.
Patient problems: No Code Available
MAUDE report 7210221 ↗InjuryDec 21, 2017Device Operates Differently Than Expected
REVISION SURGERY - DUE TO THE PATIENT HAVING A ROTATOR CUFF DEFICIENCY.
Patient problems: No Code Available
MAUDE report 7137949 ↗InjuryAug 16, 2017Device Operates Differently Than Expected
REVISION SURGERY - DUE TO ROTATOR CUFF FAILURE.
Patient problems: No Code Available
MAUDE report 6796943 ↗InjuryApr 21, 2016Inadequacy of Device Shape and/or Size
REVISION SURGERY - DUE TO THE PATIENT EXPERIENCING PAIN; THEIR SHOULDER WAS TOO TIGHT. THE SURGEON REMOVED ALL OF THE ORIGINAL IMPLANTS AND PERFORMED A REVERSE SHOULDER.
Patient problems: Pain
MAUDE report 5594498 ↗InjuryDec 23, 2015Insufficient Device Problem Information
REVISION SURGERY - DUE TO THE PATIENT'S ROTATOR CUFF TEARING; THE SURGEON CONVERTED TO A TOTAL REVERSE SHOULDER.
Patient problems: Laceration(s)
MAUDE report 5324899 ↗
Other Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer + Additive, Cemented devices
- Comprehensive Reverse Shoulder 115310Biomet Orthopedics, LLC · prosthesis, shoulder, semi-constrained, metal/polymer + additive, cemented1 death99 reports
- INHANCE 5120-00-110Depuy (Ireland) · prosthesis, shoulder, semi-constrained, metal/polymer + additive, cemented75 reports
- Comprehensive® Reverse Shoulder XL-115364Biomet Orthopedics, LLC · prosthesis, shoulder, semi-constrained, metal/polymer + additive, cemented1 recall7 reports
- Comprehensive® Reverse Shoulder XL-115366Biomet Orthopedics, LLC · prosthesis, shoulder, semi-constrained, metal/polymer + additive, cemented1 recall4 reports
- Comprehensive® Reverse Shoulder 180550Biomet Orthopedics, LLC · prosthesis, shoulder, semi-constrained, metal/polymer + additive, cemented2 deaths43 reports
- Comprehensive® Reverse Shoulder 180551Biomet Orthopedics, LLC · prosthesis, shoulder, semi-constrained, metal/polymer + additive, cemented42 reports
- DJO SURGICAL 521-07-246Encore Medical, L.P. · prosthesis, shoulder, semi-constrained, metal/polymer + additive, cemented42 reports
- Comprehensive® 110031399Zimmer, Inc. · prosthesis, shoulder, semi-constrained, metal/polymer + additive, cemented1 death36 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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