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Trident 623-00-28ERecalls & reported problems

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

All models of Trident (160)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327039399), received between Jun 6, 2017 and Jun 6, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fitting Problem” (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 16, 2026.

Most reported problems

Device problems

  • Fitting Problem1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

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

  • MalfunctionJun 6, 2017Fitting Problem; Fitting Problem

    DURING THA SURGERY, THE INSERT DID NOT FIT TO THE SHELL. THE SURGEON SCRAPED THE BONES AROUND THE CUP AND INSERTED THE ANOTHER INSERT.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 6614643 ↗

Other Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented devices

All Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented devices →

Sources and updates

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