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Trident 623-10-28CRecalls & reported problems

Howmedica Osteonics Corp. · 10 Degree Polyethylene Insert · Class 2 · Implant

Data updated Oct 13, 2026 from official FDA records · Editorial policy

Adverse event reports
3
Deaths reported
0
Injuries reported
3
Recalls naming it
0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 07613327039771), received between Mar 7, 2022 and Dec 29, 2022 — classified as 3 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (3 reports).

2 other recalls cover devices cleared under the same FDA submission (K033716); they may or may not involve this specific model.

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

  • Device Dislodged or Dislocated3
  • Unstable1

Patient problems

  • Joint Dislocation3
  • Joint Laxity1

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

  • InjuryDec 29, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated

    PATIENT HAD AN OPEN REDUCTION FOR DISLOCATION.

    Patient problems: Joint Dislocation

    MAUDE report 16068708 ↗
  • InjuryDec 22, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated

    IT WAS REPORTED BY THE HEALTH PROFESSIONAL THAT THERE IS A REVISION FOR THR. REASON FOR REVISION DUE TO DISLOCATION.

    Patient problems: Joint Dislocation

    MAUDE report 16033642 ↗
  • InjuryMar 7, 2022Unstable; Device Dislodged or Dislocated; Unstable; Device Dislodged or Dislocated

    PATIENT HAD AN INDEX LEFT THA ON (B)(6) 2021. PATIENT PRESENTED WITH INSTABILITY AND DISLOCATION OF LEFT HIP. UNDERWENT REVISION FOR INSTABILITY ON (B)(6) 2021. CUP, LINER, AND HEAD WERE EXCHANGED.

    Patient problems: Joint Dislocation; Joint Laxity

    MAUDE report 13677947 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K033716. One submission often covers many models, so check the product and lot details in each record.

  • Z-2810-2015 · Jun 25, 2015 · Terminated
    Trident 10 degrees X3 Insert 36 mm ID Catalog #623-10-36I Hip implant component
  • Z-0909-2010 · Feb 17, 2006 · Terminated
    Trident Acetabular Hip System Polyethylene Inserts, Stryker Orthopaedics, multiple sizes, Mahwah, NJ. Intended for use in cementless fixation fro use in total hip arthroplasty to

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

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

Sources and updates

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