Trident X3 Insert 723-00-44FRecalls & reported problems

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 07613327297041), received between Oct 21, 2022 and Dec 12, 2025 — 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.

• InjuryDec 12, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE FOLLOWING INFORMATION WAS PROVIDED: REVISED A RIGHT HIP DUE TO INFECTION. SURGEON PERFORMED AN I&D WITH FULL IMPLANT EXCHANGE.

  Patient problems: Unspecified Infection

  MAUDE report 23788971 ↗
• InjuryJun 5, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PERFORMED AN I&D WITH HEAD AND LINER SWAP DUE TO INFECTION OF A LEFT HIP.

  Patient problems: Unspecified Infection

  MAUDE report 22152497 ↗
• InjuryDec 11, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE FOLLOWING WAS REPORTED "REVISED A LEFT HIP DUE TO INFECTION. ALL IMPLANTS REVISED."

  Patient problems: Unspecified Infection

  MAUDE report 20909646 ↗
• InjuryJan 26, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE FOLLOWING WAS REPORTED: PERFORMED AN I&D OF A LEFT HIP WITH LINER/HEAD EXCHANGE DUE TO POSSIBLE INFECTION.

  Patient problems: Unspecified Infection

  MAUDE report 18587019 ↗
• InjuryOct 2, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE FOLLOWING WAS REPORTED: "I&D WITH HEAD/LINER EXCHANGE OF A LEFT HIP DUE TO INFECTION."

  Patient problems: Unspecified Infection

  MAUDE report 17856809 ↗
• InjuryApr 17, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  DR. PERFORMED AN I&D OF A HIP WITH HEAD/LINER EXCHANGE DUE TO POSSIBLE INFECTION. HE REDUCED FROM ORIGINAL HEAD FROM A 44 TO A 36 FOR EASE OF REDUCTION.

  Patient problems: Unspecified Infection

  MAUDE report 16758790 ↗
• InjuryOct 21, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  I&D OF A LEFT HIP ORIGINALLY DONE (B)(6) 2022 AND SWAPPED THE HEAD, LINER, SLEEVE. NO ALLEGATIONS AGAINST THE IMPLANTS MADE. PER RESPONSE: "DUE TO INFECTION"

  Patient problems: Unspecified Infection

  MAUDE report 15648769 ↗