Trident 623-00-40HRecalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 07613327025330), received between Jun 21, 2018 and Sep 30, 2022 — classified as 4 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• InjurySep 30, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  AS REPORTED: PATIENT'S RIGHT HIP WAS REVISED DUE TO INFECTION. INITIAL IMPLANT DATE WAS (B)(6) 2012 AND HEAD AND LINER SWAP WAS ON (B)(6) 2022. ALL IMPLANTS CAME OUT AS PART OF A 1 STAGE REVISION. REP CONFIRMED THAT NO FURTHER INFORMATION WILL BE RELEASED BY THE HOSPITAL OR SURGEON.

  Patient problems: Unspecified Infection

  MAUDE report 15514893 ↗
• InjurySep 30, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  WHILE GATHERING INFORMATION FOR A REVISION OF THE PATIENT'S RIGHT HIP ON (B)(6) 2022, REP WAS PROVIDED A USAGE SHEET FOR A HEAD/ LINER EXCHANGE ON (B)(6) 2022 DUE TO INFECTION. REP CONFIRMED THAT NO STRYKER REP WAS PRESENT, AND THAT NO FURTHER INFORMATION WILL BE RELEASED BY THE HOSPITAL OR SURGEON. THIS REPORT IS FOR REVISION OF THE PATIENT'S RIGHT HIP ON (B)(6) 2022.

  Patient problems: Unspecified Infection

  MAUDE report 15514592 ↗
• InjuryMay 12, 2021Adverse 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. A STAGE ONE REVISION WAS DONE, ALL IMPLANTS WERE REMOVED AND A SPACER WAS PLACED. REP CONFIRMED THAT NO FURTHER INFORMATION WILL BE RELEASED BY THE HOSPITAL OR SURGEON.

  Patient problems: Unspecified Infection

  MAUDE report 11811326 ↗
• InjuryJun 21, 2018Insufficient Device Problem Information; Insufficient Device Problem Information

  IT WAS REPORTED THAT PATIENT'S RIGHT HIP WAS REVISED DUE TO POSSIBLE INFECTION (REPORTED BY SURGEON, UNKNOWN IF CONFIRMED BY PATHOLOGY, NOT IDENTIFIED). SURGEON REVISED A CERAMIC HEAD AND SLEEVE, AND POLY LINER TO SMALLER COMPONENTS OF THE SAME TYPE.

  Patient problems: Inflammation; Injury; Reaction; Unspecified Infection

  MAUDE report 7625015 ↗