DJO SURGICAL 521-01-250Recalls & reported problems
Encore Medical, L.P. · TURON PEGGED GLENOID, SZ 50MM, eplus · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 8
- Deaths reported
- 0
- Injuries reported
- 8
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 00888912145381), received between Jun 14, 2017 and Jun 25, 2025 — classified as 8 injuries.
The most frequently reported specific device problem is “Loose or Intermittent Connection” (1 report).
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
- Appropriate Device Problem Term/Code Not Available4
- Adverse Event Without Identified Device or Use Problem3
- Loose or Intermittent Connection1
- Loosening of Implant Not Related to Bone-Ingrowth1
- Material Split, Cut or Torn1
Patient problems
- No Code Available2
- Arthralgia1
- Failure of Implant1
- Inflammation1
- Insufficient Information1
- Joint Laxity1
- Swelling1
- Unspecified Infection1
Recent adverse event reports
The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.
InjuryJun 25, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryJan 17, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryFeb 21, 2022Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - PATIENT FAILED SUBSCAP.
Patient problems: Failure of Implant
MAUDE report 13572950 ↗InjuryFeb 9, 2021Loose or Intermittent Connection; Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - DUE TO GLENOID LOOSENING.
Patient problems: Insufficient Information
MAUDE report 11304249 ↗InjuryOct 1, 2020Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - FAILED CUFF NEEDED TO CONVERT TO REVERSE. POSSIBLE INFECTION.
Patient problems: Unspecified Infection
MAUDE report 10613653 ↗InjuryApr 1, 2019Appropriate Device Problem Term/Code Not Available; Material Split, Cut or Torn
REVISION SURGERY - DUE TO INFLAMMATION AND EXTRA FLUID IN THE SHOULDER; TORN ROTATOR CUFF.
Patient problems: Inflammation; Swelling
MAUDE report 8471508 ↗InjuryFeb 25, 2019Loosening of Implant Not Related to Bone-Ingrowth
REVISION SURGERY - DUE TO LOOSE GLENOID COMPONENT AND COMPROMISED ROTATOR CUFF. THIS GAVE REASON FOR TOTAL SHOULD ARTHROPLASTY (TSA) TO BE CONVERTED TO A REVERSE TOTAL SHOULDER ARTHROPLASTY (TSA).
Patient problems: No Code Available
MAUDE report 8367654 ↗InjuryJun 14, 2017Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO THE REMOVAL OF THE PEGGED GLENOID, HUMERAL NECK, HEAD AND THE CONVERSION TO A REVERSE SHOULDER PROSTHESIS (RSP). THE SURGEON USED A TURON TO RSP CONVERSION SHELL.
Patient problems: No Code Available
MAUDE report 6641677 ↗
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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