Trident X3 Insert 723-00-32ERecalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 07613327342499), received between May 9, 2022 and Dec 3, 2025 — classified as 3 injuries.

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

Recent adverse event reports

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

• InjuryDec 3, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  POSTOPERATIVE INFECTION FOLLOWING THA. TRIDENT 2 AND INSIGNIA REMOVED ON (B)(6) 2025.

  Patient problems: Unspecified Infection

  MAUDE report 23709219 ↗
• InjuryApr 21, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE FOLLOWING WAS REPORTED: LEFT PRIMARY THR (B)(6) 2023. READMITTED VIA ED (B)(6) 2023 WITH WOUND REDNESS AND HIP ASPIRATION ON THE (B)(6) 2023. STAPH AUREUS ISOLATED. REVISION SURGERY ON THE (B)(6) 2023 TO RIMFIT/V40/BIOLOX. ANTIBIOTICS (VANCOMYCIN, RIFAMPICIN, CIPROFLOXACIN). AS PER MEDICAL RECORDS: REVISION THR. 4.5 WEEKS POST PRIMARY THR WITH ACUTE S AUREUS INFECTION. DISCUSSED AT MDT FOR FULL REVISION RETAINING DISTAL CEMENT MANTLE. POST APP EXCISING OLD SCAR. ALMOST FORMING SINUS. ALL DEBRIDED. VERY CONTAMINATED ALL THE WAY TO JOINT. POST REPAIR PARTIALLY FAILED.

  Patient problems: Bacterial Infection

  MAUDE report 16783203 ↗
• InjuryMay 9, 2022Unstable; Unstable

  THE FOLLOWING WAS REPORTED: UNSTABLE TOTAL RIGHT HIP. POLY LINER EXCHANGE TO MDM CONSTRUCT.

  Patient problems: Ambulation or Postural Difficulties

  MAUDE report 14342739 ↗