Trident 623-00-28DRecalls & reported problems

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 07613327039382), received between Apr 5, 2017 and Jul 11, 2025 — classified as 6 injuries, 1 malfunction.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (3 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 7 most recent of 7 reports, in the reporter's own words as published by the FDA.

• InjuryJul 11, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PAIN IN LEFT THIGH AND GROIN.

  Patient problems: Pain

  MAUDE report 22477323 ↗
• InjuryJul 28, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated

  THIS REPORT IS FOR THE INTERVENTION FOR DISLOCATION ON (B)(6) 2021. NO DEVICES WERE REVISED. TOTAL HIP REPLACEMENT LEFT ON (B)(6) 2012 IN (B)(6) STUDY. LUXATION OF THE HIP ON (B)(6) 2017 AND AGAIN ON (B)(6) 2021. REPOSITIONED AND RESOLVED. UPDATE PER SALES REP: "THESE WERE NO SURGERIES, THE HIP WAS REPOSITIONED TWICE."

  Patient problems: Joint Dislocation

  MAUDE report 17412980 ↗
• InjuryJul 28, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated

  THIS REPORT IS FOR THE INTERVENTION FOR DISLOCATION ON (B)(6) 2017. NO DEVICES WERE REVISED. TOTAL HIP REPLACEMENT LEFT ON (B)(6) 2012 IN ATX STUDY. LUXATION OF THE HIP ON (B)(6) 2017 AND AGAIN ON (B)(6) 2021. REPOSITIONED AND RESOLVED. UPDATE PER SALES REP: "THESE WERE NO SURGERIES, THE HIP WAS REPOSITIONED TWICE."

  Patient problems: Joint Dislocation

  MAUDE report 17412860 ↗
• InjuryNov 16, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT STATED THEY HAD PAIN IN THEIR RIGHT HIP AND WERE NOT SATISFIED WITH THEIR RIGHT HIP REPLACEMENT.

  Patient problems: Pain

  MAUDE report 15806155 ↗
• InjuryFeb 20, 2019Device Dislodged or Dislocated; Device Dislodged or Dislocated

  POST-OPERTIVE DIAGNOSIS: PATIENT UNDERWENT PRIMARY RIGHT TOTAL HIP REPLACEMENT (B)(6) 2018. PATIENT RETURNED FOR INSTABILITY WITH TWO ANTERIOR DISLOCATIONS. PATIENT WAS REVISED ON (B)(6) 2018. ALL COMPONENTS EXCHANGED EXCEPT FEMUR.

  Patient problems: Injury; Joint Dislocation

  MAUDE report 8356606 ↗
• InjuryJun 13, 2018Insufficient Device Problem Information; Insufficient Device Problem Information

  THE CUSTOMER REPORTED THAT THE PATIENT WHO HAD BEEN IMPLANTED WITH STRYKER DEVICES DEVELOPED AN INFECTION.

  Patient problems: Unspecified Infection

  MAUDE report 7597422 ↗
• MalfunctionApr 5, 2017Fitting Problem; Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE TRIDENT X3 LINER WAS NOT FITTED IN THE TRIDENT CUP. THEREFORE, THE LINER WAS CHANGED WITH A NEW ONE AND THE OPERATION WAS SUCCESSFUL.

  Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient

  MAUDE report 6460582 ↗