Skip to content

Optetrak Logic 02-010-04-0335Recalls & reported problems

Exactech, Inc. · Class 2 · Implant

All models of Optetrak Logic (408)

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 10885862158383), received between Oct 7, 2019 and Oct 7, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Material Rupture” (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
  • Material Rupture1
  • Unstable1

Patient problems

  • Joint Laxity1
  • Muscle/Tendon Damage1
  • No Information1

Recent adverse event reports

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

  • InjuryOct 7, 2019Material Rupture; Unstable; Appropriate Device Problem Term/Code Not Available

    REVISED DUE TO INSTABILITY ¿ RUPTURED POSTERIOR CRUCIATE LIGAMENT (PCL), REVISED TO HINGE. THE PATIENT WAS STABLE AS THEY LEFT THE OPERATING ROOM. THERE WAS NO DELAY TO THE SURGERY. THE REP WAS PRESENT AT THE TIME OF THE SURGERY.

    Patient problems: Joint Laxity; Muscle/Tendon Damage; No Information

    MAUDE report 9163187 ↗

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

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