DJO SURGICAL 521-01-254Recalls & reported problems
Encore Medical, L.P. · TURON PEGGED GLENOID, SZ 54MM, eplus · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 5
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00888912145404), received between Nov 16, 2017 and Jun 4, 2024 — classified as 5 injuries.
The most frequently reported specific device problem is “Device Operates Differently Than Expected” (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 Problem2
- Device Operates Differently Than Expected2
- Therapeutic or Diagnostic Output Failure1
- Unstable1
Patient problems
- Failure of Implant2
- Insufficient Information2
- No Code Available1
- Pain1
- Unspecified Infection1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
InjuryJun 4, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO DR. REVISED THIS PATIENT FROM A TURON TSA TO A REVERSE TSA BECAUSE OF A FAILED ROTATOR CUFF.
Patient problems: Insufficient Information; Unspecified Infection
MAUDE report 19464331 ↗InjuryDec 20, 2021Therapeutic or Diagnostic Output Failure
InjuryAug 3, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO A FAILED TURON SHOULDER. IT REQUIRED A REVERSE TOTAL SHOULDER.
Patient problems: Failure of Implant; Insufficient Information
MAUDE report 7747832 ↗InjuryJan 8, 2018Device Operates Differently Than Expected
REVISION SURGERY - DUE TO A FAILED TOTAL SHOULDER. THE SURGEON CONVERTED IT TO A REVERSE.
Patient problems: No Code Available
MAUDE report 7172685 ↗InjuryNov 16, 2017Unstable; Device Operates Differently Than Expected
REVISION SURGERY - DUE TO A FAILED TOTAL SHOULDER. A REVERSE WAS REQUIRED FOR STABILITY.
Patient problems: Failure of Implant
MAUDE report 7038130 ↗
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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