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Trident 623-10-32HRecalls & reported problems

Howmedica Osteonics Corp. · 10 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 07613327039887), received between Oct 22, 2018 and Oct 22, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Difficult to Insert” (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

  • Difficult to Insert1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionOct 22, 2018Difficult to Insert; Difficult to Insert

    SURGEON PROVIDING THE SURGERY CLAIMED: DESPITE THE USE OF THE CORRECT SURGICAL TECHNIQUE, IMPLANTATION OF THE INSERT WAS IMPOSSIBLE (SEVERAL ATTEMPTS). AS A RESULT, A SECOND IMPLANT WAS USED. DURING SURGERY THE SURGEON DECIDED TO USE A INSERT 28H INSTEAD OF 32H REPLACEMENT WAS AVAILABLE.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 7990254 ↗

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

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Sources and updates

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