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Trident X3 Insert 763-10-36ERecalls & reported problems

Howmedica Osteonics Corp. · Trident X3 10 Degree Eccentric Insert · Class 2 · Implant

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 07613327339222), received between Sep 15, 2022 and Sep 15, 2022 — classified as 1 injury.

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Unstable1

Patient problems

  • Joint Laxity1

Recent adverse event reports

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

  • InjurySep 15, 2022Unstable; Unstable

    REVISED LEFT HIP CUP, LINER AND HEAD DUE TO INSTABILITY. THIS TIME, THE PATIENT WAS CHANGED TO CONSTRAINED LINER WITH MULTI-HOLE CUP. NO ALLEGATIONS MADE AGAINST THE IMPLANTS.

    Patient problems: Joint Laxity

    MAUDE report 15427673 ↗

Other Prosthesis, hip, semi-constrained, metal/polymer, cemented devices

All Prosthesis, hip, semi-constrained, metal/polymer, cemented devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.