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Truliant 02-020-14-0230Recalls & reported problems

Exactech, Inc. · Truliant CR Porous Femoral · 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 10885862315007), received between Nov 13, 2020 and Nov 13, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Material Fragmentation” (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

  • Material Fragmentation1

Patient problems

  • Device Embedded In Tissue or Plaque1

Recent adverse event reports

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

  • InjuryNov 13, 2020Material Fragmentation; Material Fragmentation

    AS REPORTED, AFTER THE LEFT TKA, IN THE POST OP X-RAYS, POROUS BEADS DISLODGED FROM IMPLANT AND ARE SEEN ON X-RAY FOLLOWING THE CASE. PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION FOLLOWING THE EVENT DEVICE NOT RETURNING AS IT WAS IMPLANTED.

    Patient problems: Device Embedded In Tissue or Plaque

    MAUDE report 10837203 ↗

Other Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer devices

All Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer devices →

Sources and updates

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