Trident 623-00-32CRecalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 07613327025354), received between Mar 5, 2018 and Jun 26, 2026 — classified as 5 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (2 reports).

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 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• InjuryJun 26, 2026Unstable; Naturally Worn

  REVISED A STRYKER HIP (LEFT). THIS COMPONENT IS BEING REVISED DUE TO INSTABILITY. VISIBLE SIGNS OF DAMAGE & WEAR TO THE POLY. A HEAD AND LINER WERE REVISED.

  Patient problems: Ambulation or Postural Difficulties

  MAUDE report 25642272 ↗
• InjuryAug 16, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated

  THIS PI IS FOR THE CLOSED REDUCTION ON (B)(6) 2022. PATIENT HAD AN INDEX LEFT THA ON (B)(6) 2022. PATIENT HAD INSTABILITY AND DISLOCATED, REQUIRING CLOSED REDUCTION UNDER ANESTHESIA ON (B)(6) 2022. PATIENT CONTINUED WITH INSTABILITY AND UNDERWENT REVISION ON (B)(6) 2022. ALL COMPONENTS WERE EXCHANGED EXCEPT THE STEM.

  Patient problems: Ambulation or Postural Difficulties

  MAUDE report 17555148 ↗
• InjurySep 19, 2019Insufficient Device Problem Information; Insufficient Device Problem Information

  PATIENT IS PART OF THE TRITANIUM PRIMARY ACETABULAR SHELL STUDY AND REPORTED PAIN IN THE STUDY HIP DURING THE 6-YEAR VISIT. SHE REPORTED OCCASIONAL STIFFNESS UPON RISING OR AFTER SITTING FOR LONG PERIODS OF TIME.

  Patient problems: Pain

  MAUDE report 9087587 ↗
• InjurySep 25, 2018Insufficient Device Problem Information; Insufficient Device Problem Information

  PRIMARY SURGERY AGAINST OSTEOARTHRITIS WITH TRIDENT, ACCOLADE AND DELTA CERAMIC HEAD WAS PERFORMED ON (B)(6) 2018. THEN, REMOVAL SURGERY WAS PERFORMED AND MOLD TYPE CEMENT SPACER WAS IMPLANTED ON (B)(6) 2018 DUE TO INFECTION OF IMPLANTED SITE. LESION: LEFT HIP.

  Patient problems: Injury; Unspecified Infection

  MAUDE report 7908409 ↗
• InjuryMar 5, 2018Device Dislodged or Dislocated; Device Dislodged or Dislocated

  PATIENT HAD A COMPETITOR COMPRESSION HIP SCREW REVISED TO A STRYKER RELIANCE CEMENTED TOTAL HIP ON (B)(6) 2017. SHE SUBSEQUENTLY FELL AND DISLOCATED. THE SURGEON DETERMINED THE PATIENT WOULD BENEFIT FROM A CONVERSION TO AN MDM LINER AND HEAD. THE OPERATION WAS COMPLETED SUCCESSFULLY. THE PATIENT WAS STABLE THROUGH THE FULL RANGE OF MOTION. SURGEON ALLEGES NO DEFECT WITH STRYKER COMPONENTS, STATING THAT PATIENT FACTORS CONTRIBUTED TO THE DISLOCATIONS.

  Patient problems: Fall; Injury; Joint Dislocation

  MAUDE report 7312615 ↗