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

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 07613327342710), received between Apr 13, 2023 and May 21, 2026 — classified as 7 injuries.

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

Recent adverse event reports

The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.

• InjuryMay 21, 2026Adverse Event Without Identified Device or Use Problem

  THE FOLLOWING INFORMATION WAS PROVIDED: IT WAS REPORTED THAT: ASEPTIC LOOSENING, INFECTION OF HIP JOINT POST-OPERATIVELY.

  Patient problems: Unspecified Infection

  MAUDE report 25240256 ↗
• InjuryDec 16, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THIS PI IS FOR THE I&D PERFORMED ON (B)(6) 2023. LEFT HIP. THIS SUBJECT EXPERIENCED PROLONGED WOUND DEHISCENCE RELATED TO A MEDICATION REGIMEN TO TREAT HER RA. CULTURES WERE INITIALLY NEGATIVE BUT THEN CAME BACK POSITIVE FOR PYODERMA GANGRENOSUM. SHE FIRST PRESENTED INTO CLINIC ON (B)(6) 2023 WITH DELAYED HEALING. AT THE NEXT VISIT (ON (B)(6) 2023) DR. DECIDED TO SCHEDULE THE SUBJECT FOR A POSSIBLE REVISION SURGERY. ON (B)(6) 2023 DR. PERFORMED AND I&D AND APPLIED AN INCISIONAL WOUND VAC. SHE CONTINUED TO FOLLOW UP WITH ONGOING COMPLAINTS UNTIL ON (B)(6) 2024. ON THAT DATE, THE SUBJECT COMPLETED A FOLLOW-UP QUESTIONNAIRE AND INDICATED SHE WAS NOT SATISFIED WITH HER STUDY HIP REPLACEMENT. SHE CITED THE REASONS OF "SORENESS" AND "HEALING IS STILL ONGOING." DR. OPINED THAT THIS WOUND RELATED EVENT WAS NOT RELATED TO THE DEVICE NOR PROCEDURE.

  Patient problems: Discomfort; Pain; Unspecified Infection; Wound Dehiscence

  MAUDE report 20937308 ↗
• InjuryDec 16, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THIS PI IS FOR THE ONGOING ISSUES AFTER I&D. LEFT HIP. THIS SUBJECT EXPERIENCED PROLONGED WOUND DEHISCENCE RELATED TO A MEDICATION REGIMEN TO TREAT HER RA. CULTURES WERE INITIALLY NEGATIVE BUT THEN CAME BACK POSITIVE FOR PYODERMA GANGRENOSUM. SHE FIRST PRESENTED INTO CLINIC ON (B)(6) 2023 WITH DELAYED HEALING. AT THE NEXT VISIT (ON (B)(6) 2023) DR DECIDED TO SCHEDULE THE SUBJECT FOR A POSSIBLE REVISION SURGERY. ON (B)(6) 2023 DR. PERFORMED AND I&D AND APPLIED AN INCISIONAL WOUND VAC. SHE CONTINUED TO FOLLOW UP WITH ONGOING COMPLAINTS UNTIL ON (B)(6) 2024. ON THAT DATE, THE SUBJECT COMPLETED A FOLLOW-UP QUESTIONNAIRE AND INDICATED SHE WAS NOT SATISFIED WITH HER STUDY HIP REPLACEMENT. SHE CITED THE REASONS OF "SORENESS" AND "HEALING IS STILL ONGOING." DR. OPINED THAT THIS WOUND RELATED EVENT WAS NOT RELATED TO THE DEVICE NOR PROCEDURE.

  Patient problems: Discomfort; Fatigue; Pain; Wound Dehiscence

  MAUDE report 20937307 ↗
• InjuryJun 12, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT'S LEFT HIP WAS REVISED DUE TO ILIOPSOAS INJURY (REP CONFIRMED INJURY WAS NOT IMPLANT-RELATED). ILIOPSOAS RELEASE WAS PERFORMED, AND A POLY LINER AND CERAMIC HEAD WERE REVISED TO AN MDM METAL LINER, ADM/MDM POLY INSERT, AND METAL FEMORAL HEAD. REP CONFIRMED THAT NO FURTHER INFORMATION WILL BE RELEASED BY THE HOSPITAL OR SURGEON.

  Patient problems: Muscle/Tendon Damage

  MAUDE report 19519577 ↗
• InjuryApr 25, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT'S RIGHT HIP AFTER PATIENT COMPLAINT OF FEMORAL PAIN. SURGEON ORIGINALLY SUSPECTED A LOOSE STEM. HOWEVER, INTRA-OPERATIVELY, STEM WAS CONFIRMED AS WELL-FIXED. AN ACCOLADE II STEM, HEAD, AND LINER WERE REVISED TO A RESTORATION MODULAR STEM CONSTRUCT, NEW HEAD, ADM/MDM POLY INSERT, AND MDM METAL LINER (SURGEON REPORTED HE WANTED A DUAL MOBILITY LINER IN THE PATIENT. THERE ARE NO ALLEGATIONS AGAINST THE REVISED LINER OR HEAD). REP CONFIRMED THAT NO FURTHER INFORMATION WILL BE RELEASED BY THE HOSPITAL OR SURGEON.

  Patient problems: Pain

  MAUDE report 19184814 ↗
• InjuryMar 26, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE PATIENT UNDERWENT HEAD AND LINER REPLACEMENT DUE TO THA POSTOPERATIVE INFECTION.

  Patient problems: Unspecified Infection

  MAUDE report 18977135 ↗
• InjuryApr 13, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT'S RIGHT HIP WAS REVISED DUE TO INFECTION (SURGEON REPORTED THAT AFTER PATIENT FELL, A HEMATOMA DEVELOPED AND BECAME INFECTED). A STAGE 1 REVISION WAS PERFORMED WHERE ALL IMPLANTS WERE REMOVED AND A SPACER WAS PLACED.

  Patient problems: Bursitis; Muscle/Tendon Damage; Numbness; Skin Discoloration; Swelling/ Edema; Unspecified Infection

  MAUDE report 16729632 ↗