Trident X3 Insert 723-00-40FRecalls & reported problems

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 07613327342727), received between Oct 24, 2022 and Sep 24, 2026 — classified as 6 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. 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 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

• InjurySep 24, 2026Adverse Event Without Identified Device or Use Problem

  Patient problems: Unspecified Infection

  MAUDE report 50876495 ↗
• InjurySep 11, 2026Unstable

  The following information was provided: Revised a right hip due to instability. Revised previously from a competitor hip to a Stryker cup w 40 liner. He now revised the liner to a constrained.

  Patient problems: Joint Laxity

  MAUDE report 50729628 ↗
• InjuryMar 31, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PERFORMED AN I&D HEAD/LINER EXCHANGE DUE TO INFECTION OF A RIGHT HIP.

  Patient problems: Unspecified Infection

  MAUDE report 21730315 ↗
• InjuryJun 15, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  AS REPORTED: "PATIENT'S LEFT HIP WAS REVISED DUE TO INFECTION. ALL IMPLANTS PULLED. PATIENT HAS HAD PRIOR REVISIONS.

  Patient problems: Unspecified Infection

  MAUDE report 17140762 ↗
• InjuryFeb 15, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  I&D OF OF A LEFT HIP DUE TO INFECTION. ORIGINAL SURGERY DATE WAS (B)(6) 2023. REVISED THE LINER IN THE PROCESS.

  Patient problems: Unspecified Infection

  MAUDE report 16377287 ↗
• InjuryOct 24, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT REPORTED A RIGHT HIP REPLACEMENT ON (B)(6) 2021 AND REPORTED PAIN. PATIENT INQUIRED ABOUT A RECALL. THIS PI FOR LEFT HIP.

  Patient problems: Inflammation; Pain

  MAUDE report 15657058 ↗