Trident 623-10-32GRecalls & reported problems

Summary

The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 07613327039870), received between Feb 27, 2018 and May 17, 2023 — classified as 7 injuries, 1 malfunction.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (6 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.

• InjuryMay 17, 2023Device Dislodged or Dislocated; Insufficient Device Problem Information; Device Dislodged or Dislocated; Insufficient Device Problem Information

  THE PATIENTS LINER AND HEAD WAS REVISED. ADDITIONAL INFORMATION: IT WAS REPORTED THAT DURING FIRST REVISION THAT THE ABDUCTORS WERE INSUFFICIENT. PATIENT WAS LEANING AWKWARDLY OUT OF HIS BED REACHING FOR A LIGHT SWITCH WHEN THE IMPLANT DISLOCATED ON THIS OCCASION. AFTER THE IMPLANTATION OF THE MDM LINER AND NEW FEMORAL HEAD IN THIS CASE, SHE COMPLETED A GLUTEUS MAX TRANSFER TO REPLACE ABDUCTORS.

  Patient problems: Insufficient Information; Joint Dislocation

  MAUDE report 16945172 ↗
• InjuryJan 9, 2020Insufficient Device Problem Information; Insufficient Device Problem Information

  PATIENT HAD A HIP DISLOCATION. SEEN BY THE DR IN (B)(6) 2018.

  Patient problems: Joint Dislocation

  MAUDE report 9569112 ↗
• InjuryApr 29, 2019Device Dislodged or Dislocated; Device Dislodged or Dislocated

  BASED ON OUTPATIENT MEDICAL RECORDS THE FOLLOWING WAS REPORTED. "PATIENT WAS VERY HAPPY WITH THIS BUT HAD A FALL BACK IN JUNE SUSTAINING A POSTERIOR DISLOCATION OF HIS HIP. THIS WAS REDUCED IN ED. SINCE THEN IT HAS COME OUT THREE FURTHER TIMES, IN EACH CASE IT WAS REDUCED IN ED." THIS IS FOR CLOSED REDUCTION 4 OF 4.

  Patient problems: Fall

  MAUDE report 8561839 ↗
• InjuryApr 29, 2019Device Dislodged or Dislocated; Device Dislodged or Dislocated

  BASED ON OUTPATIENT MEDICAL RECORDS THE FOLLOWING WAS REPORTED. "PATIENT WAS VERY HAPPY WITH THIS BUT HAD A FALL BACK IN JUNE SUSTAINING A POSTERIOR DISLOCATION OF HIS HIP. THIS WAS REDUCED IN ED. SINCE THEN IT HAS COME OUT THREE FURTHER TIMES, IN EACH CASE IT WAS REDUCED IN ED." THIS IS FOR CLOSED REDUCTION 2 OF 4.

  Patient problems: Fall

  MAUDE report 8561838 ↗
• InjuryApr 29, 2019Device Dislodged or Dislocated; Device Dislodged or Dislocated

  BASED ON OUTPATIENT MEDICAL RECORDS THE FOLLOWING WAS REPORTED. "HE WAS VERY HAPPY WITH THIS BUT HAD A FALL BACK IN (B)(6) SUSTAINING A POSTERIOR DISLOCATION OF HIS HIP. THIS WAS REDUCED IN ED. SINCE THEN IT HAS COME OUT THREE FURTHER TIMES, IN EACH CASE IT WAS REDUCED IN ED." THIS IS FOR CLOSED REDUCTION 3 OF 4.

  Patient problems: Fall

  MAUDE report 8561836 ↗
• InjuryApr 29, 2019Device Dislodged or Dislocated; Device Dislodged or Dislocated

  BASED ON OUTPATIENT MEDICAL RECORDS THE FOLLOWING WAS REPORTED. "PATIENT WAS VERY HAPPY WITH THIS BUT HAD A FALL BACK IN JUNE SUSTAINING A POSTERIOR DISLOCATION OF HIP. THIS WAS REDUCED IN ED. SINCE THEN IT HAS COME OUT THREE FURTHER TIMES, IN EACH CASE IT WAS REDUCED IN ED." THIS IS FOR CLOSED REDUCTION 1 OF 4.

  Patient problems: Fall

  MAUDE report 8561678 ↗
• InjuryFeb 6, 2019Device Dislodged or Dislocated; Device Dislodged or Dislocated

  BOOKED REVISION CASE DUE TO DISLOCATION POST PREVIOUS FRACTURE. HEAD AND LINER REVISED FROM +0 HEAD TO +8 HEAD AND MDM. MDM TRIALED ON TABLE AND CASE COMPLETED. THIS PI IS FOR THE DISLOCATION.

  Patient problems: Injury

  MAUDE report 8311368 ↗
• MalfunctionFeb 27, 2018Device Operates Differently Than Expected; Device Operates Differently Than Expected

  DURING SURGERY THE PLASTIC LINER POPPED LOOSE. THIS WAS A PLASTIC LINER USED WITH TRIDENT. THE SURGEON COULDN¿T TELL IF HE WAS RESPONSIBLE OR MALFUNCTIONING. IT HAPPENED WHEN HE WAS ABOUT TO TRIAL THE HIP. A NEW LINER WAS INSERTED AND THE OPERATION CONTINUED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7299289 ↗