DJO SURGICAL 520-54-022Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888912145244), received between Jan 14, 2016 and Jan 14, 2016 — classified as 1 injury.

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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryJan 14, 2016Insufficient Device Problem Information

  REVISION SURGERY - DUE TO THE PATIENT TEARING HIS CUFF MUSCLES AND NEEDING TO BE REVISED.

  Patient problems: No Code Available

  MAUDE report 5367235 ↗

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-0799-2011 · Nov 5, 2010 · Terminated
  Turon Shoulder System Instrumentation, Turon Trial Humeral Neck, DJO Surgical
• 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