DJO SURGICAL 520-46-120Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00888912025041), received between Sep 29, 2015 and May 6, 2022 — classified as 4 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).

4 other recalls cover devices cleared under the same FDA submission (K080402); they may or may not involve this specific model.

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.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• InjuryMay 6, 2022Appropriate Device Problem Term/Code Not Available

  REVISION SURGERY - DUE TO DISLOCATION.

  Patient problems: Joint Dislocation

  MAUDE report 14306976 ↗
• InjuryDec 5, 2017Loose or Intermittent Connection

  REVISION SURGERY - DUE TO THE PATIENT COMPLAINING OF PAIN. POSSIBLE GLENOID LOOSENING.

  Patient problems: No Code Available; Pain

  MAUDE report 7083098 ↗
• InjuryJan 22, 2016Appropriate Device Problem Term/Code Not Available

  REVISION SURGERY - DUE TO SUB SCAP FAILURE.

  Patient problems: Failure of Implant

  MAUDE report 5385391 ↗
• InjurySep 29, 2015Insufficient Device Problem Information

  REVISION SURGERY - DUE TO THE PATIENT FALLING AND EXPERIENCING PAIN. THE SURGEON REMOVED THE OLD HEAD AND NECK, WASHED OUT THE SHOULDER, ADDED A 46 GLENOID NECK AND NEW HEAD.

  Patient problems: Fall; Pain

  MAUDE report 5112189 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K080402. One submission often covers many models, so check the product and lot details in each record.

• Z-0801-2011 · Nov 5, 2010 · Terminated
  Turon Shoulder System Instrumentation, Turon Pegged Glenoid Drill Guide, REF 804-25-024, DJO Surgical
• Z-0798-2011 · Nov 5, 2010 · Terminated
  Turon Shoulder System Instrumentation, Turon Humeral Head Trials, DJO Surgical
• Z-0800-2011 · Nov 5, 2010 · Terminated
  Turon Shoulder System Instrumentation, Turon Trial Pegged Glenoid, DJO Surgical
• Z-0799-2011 · Nov 5, 2010 · Terminated
  Turon Shoulder System Instrumentation, Turon Trial Humeral Neck, DJO Surgical