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DJO SURGICAL 520-40-316Recalls & reported problems

Encore Medical, L.P. · AltiVate Anatomic, Offset Humeral Head, 40X16 · Class 2 · Implant

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00190446176183), received between Oct 1, 2020 and Jul 27, 2022 — classified as 2 injuries.

The most frequently reported specific device problem is “Unstable” (1 report).

6 other recalls cover devices cleared under the same FDA submission (K162024); 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

Device problems

  • Appropriate Device Problem Term/Code Not Available1
  • Unstable1

Patient problems

  • Insufficient Information1
  • Joint Dislocation1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjuryJul 27, 2022Unstable

    REVISION SURGERY - DUE TO DISLOCATION AND INSTABILITY.

    Patient problems: Joint Dislocation

    MAUDE report 15117174 ↗
  • InjuryOct 1, 2020Appropriate Device Problem Term/Code Not Available

    REVISION SURGERY - SURGEON EXPLANTED BUT DID NOT IMPLANT ANYTHING.

    Patient problems: Insufficient Information

    MAUDE report 10613650 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K162024. One submission often covers many models, so check the product and lot details in each record.

  • Z-2331-2021 · Jun 28, 2021 · Open, Classified
    AltiVate Anatomic Shoulder System for the following Part Numbers: 1. Part # 520-08-00, Rev. C., 2. Part # 520-10-000, 3. Part # 520-12-000, 4. Part # 520-14-000, 5. Part # 520-16
  • Z-1258-2018 · Jan 29, 2018 · Completed
    Altivate Anatomic(TM) INSTRUMENTATION, PEGGED GLENOID TRIAL, SIZE 46mm, REF 804-07-460 Product Usage: The AltiVate Anatomic Shoulder System is a total shoulder system indicated as
  • Z-1257-2018 · Jan 29, 2018 · Completed
    Altivate Anatomic(TM) INSTRUMENTATION, PEGGED GLENOID TRIAL, SIZE 42mm, REF 804-07-420 Product Usage: The AltiVate Anatomic Shoulder System is a total shoulder system indicated as
  • Z-1260-2018 · Jan 29, 2018 · Completed
    Altivate Anatomic(TM) INSTRUMENTATION, PEGGED GLENOID TRIAL, SIZE 54mm, REF 804-07-540 Product Usage: The AltiVate Anatomic Shoulder System is a total shoulder system indicated
  • Z-1259-2018 · Jan 29, 2018 · Completed
    Altivate Anatomic(TM) INSTRUMENTATION, PEGGED GLENOID TRIAL, SIZE 50mm, REF 804-07-500 Product Usage: The AltiVate Anatomic Shoulder System is a total shoulder system indicated as
  • Z-1256-2018 · Jan 29, 2018 · Completed
    Altivate Anatomic(TM) INSTRUMENTATION, PEGGED GLENOID TRIAL, SIZE 38mm, REF 804-07-380 Product Usage: The AltiVate Anatomic Shoulder System is a total shoulder system indicated as

Other PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED devices

All PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page