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Trident X3 Insert 723-00-32CRecalls & reported problems

Howmedica Osteonics Corp. · Trident X3 0 Degree Polyethylene Insert · Class 2 · Implant

All models of Trident X3 Insert (22)

Data updated Oct 16, 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 07613327297027), received between Jan 6, 2023 and Jan 6, 2023 — classified as 1 injury.

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 16, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Unspecified Infection1

Recent adverse event reports

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

  • InjuryJan 6, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    AS REPORTED: "RIGHT HIP I&D WITH POSSIBLE COMPONENT CHANGE. PRE-OP DIAGNOSIS: INFECTION RIGHT HIP. NO FURTHER INFORMATION AVAILABLE PER HOSPITAL" ALL IMPLANTS WERE REMOVED.

    Patient problems: Unspecified Infection

    MAUDE report 16118694 ↗

Other PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED devices

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Sources and updates

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