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DJO SURGICAL 292-13-708Recalls & reported problems

Encore Medical, L.P. · MOVATION TIBIAL INSERT, SIZE 8, 13mm VE · 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 00888912112796), received between Sep 17, 2015 and Nov 21, 2018 — classified as 2 injuries.

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

  • Adverse Event Without Identified Device or Use Problem1
  • Unstable1

Patient problems

  • Ambulation or Postural Difficulties1
  • No Code Available1

Recent adverse event reports

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

  • InjuryNov 21, 2018Adverse Event Without Identified Device or Use Problem

    REVISION SURGERY - DUE TO WASHOUT AND POLY SWAP.

    Patient problems: No Code Available

    MAUDE report 8096399 ↗
  • InjurySep 17, 2015Unstable

    REVISION SURGERY: THE PATIENT WAS UNSTABLE DUE TO THE POLY INSERT; THE SURGEON DECIDED THE PATIENT NEEDED A THICKER INSERT.

    Patient problems: Ambulation or Postural Difficulties

    MAUDE report 5084986 ↗

Other PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER devices

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

Sources and updates

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