Skip to content

Truliant 02-020-11-0315Recalls & reported problems

Exactech, Inc. · Class 2 · Implant

All models of Truliant (414)

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 10885862314512), received between Aug 5, 2022 and Aug 5, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Fracture” (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
  • Fracture1

Patient problems

  • Bone Fracture(s)1
  • Periprosthetic fracture1

Recent adverse event reports

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

  • InjuryAug 5, 2022Fracture; Adverse Event Without Identified Device or Use Problem; Fracture; Adverse Event Without Identified Device or Use Problem

    AS REPORTED, THIS 79 YEAR OLD, FEMALE PATIENT HAD AN INITIAL RIGHT SIDE TKA ON (B)(6) 2019. THE PATIENT PRESENTED WITH A L DISTAL FEMUR FX ON (B)(6) 2019 AND WAS REVISED ON (B)(6) 2019. OUTCOME: RESOLVED.

    Patient problems: Bone Fracture(s); Periprosthetic fracture

    MAUDE report 15173682 ↗

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