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Trident 690-00-32JRecalls & reported problems

Howmedica Osteonics Corp. · Constrained Acetabular Insert · Class 2 · Implant

All models of Trident (160)

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

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327025576), received between Jan 16, 2022 and May 31, 2022 — classified as 2 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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

  • Adverse Event Without Identified Device or Use Problem1
  • Device Dislodged or Dislocated1
  • Mechanical Problem1

Patient problems

  • Ambulation or Postural Difficulties2
  • Pain2
  • Joint Dislocation1
  • Loss of Range of Motion1
  • Unspecified Infection1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjuryMay 31, 2022Mechanical Problem; Mechanical Problem

    PATIENT WAS FIRST IMPLANTED WITH STRYKER IMPLANTS ON (B)(6) 2017, HE WAS REVISED ON (B)(6) 2017 DUE TO INFECTION. PATIENT THEN UNDERWENT SURGERY ON (B)(6) 2018 TO ADDRESS RECURRENT DISLOCATIONS AND CONTINUED INFECTION WHEREBY SUBTOTAL SYNOVECTOMY, HETEROTOPIC OSSIFICATION RESECTION, QUADRICEPSPLASTY, GLUTEUS TENOTOMY WITH REPAIR INSERTION ABX DELIVERY SYSTEM, XENOGRAFT 500MG WERE CARRIED OUT. NO COMPONENTS WERE REPORTED TO BE REVISED DURING THIS PROCEDURE. THE PATIENT HAD A POSITIVE SCREEN FOR MRSA FROM A NASAL SWAB. PATIENT IS STILL EXPERIENCING PAIN AND RANGE OF MOTION ISSUES. PATIENT'S SURGEON IS RECOMMENDING AMPUTATION. THIS IS FOR PAIN/ROM AFTER 2018 MEDICAL INTERVENTION.

    Patient problems: Ambulation or Postural Difficulties; Loss of Range of Motion; Pain

    MAUDE report 14554200 ↗
  • InjuryJan 16, 2022Device Dislodged or Dislocated; Adverse Event Without Identified Device or Use Problem; Device Dislodged or Dislocated; Adverse Event Without Identified Device or Use Problem

    PATIENT WAS FIRST IMPLANTED WITH STRYKER IMPLANTS ON (B)(6) 2017, HE WAS REVISED ON (B)(6) 2017 DUE TO INFECTION. PATIENT THEN UNDERWENT SURGERY ON (B)(6) 2018 TO ADDRESS RECURRENT DISLOCATIONS AND CONTINUED INFECTION WHEREBY SUBTOTAL SYNOVECTOMY, HETEROTOPIC OSSIFICATION RESECTION, QUADRICEPSPLASTY, GLUTEUS TENOTOMY WITH REPAIR INSERTION ABX DELIVERY SYSTEM, ACELL XENOGRAFT 500MG WERE CARRIED OUT. NO COMPONENTS WERE REPORTED TO BE REVISED DURING THIS PROCEDURE. THE PATIENT HAD A POSITIVE SCREEN FOR MRSA FROM A NASAL SWAB. PATIENT IS STILL EXPERIENCING PAIN AND RANGE OF MOTION ISSUES. PATIENT'S SURGEON IS RECOMMENDING AMPUTATION. THIS IS FOR SURGERY ON (B)(6) 2018.

    Patient problems: Ambulation or Postural Difficulties; Joint Dislocation; Pain; Unspecified Infection

    MAUDE report 13262659 ↗

Other Prosthesis, hip, constrained, cemented or uncemented, metal/polymer devices

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Sources and updates

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