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DJO SURGICAL 360-13-512Recalls & reported problems

Encore Medical, L.P. · INSERT, POSTERIOR STABILIZED, SERIES 500, SIZE12 13MM CM · Class 2 · Implant

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

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888912116442), received between Sep 20, 2019 and Sep 20, 2019 — classified as 1 injury.

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

Most reported problems

Device problems

  • Appropriate Device Problem Term/Code Not Available1
  • Unstable1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

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

  • InjurySep 20, 2019Unstable; Appropriate Device Problem Term/Code Not Available

    REVISION SURGERY - PATIENT HAD INSTABILITY.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 9099483 ↗

Other Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer devices

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Sources and updates

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