Trident 623-00-40GRecalls & reported problems

Summary

The FDA's MAUDE database contains 10 adverse event reports that list this exact device (DI 07613327025361), received between Apr 18, 2018 and Nov 27, 2024 — classified as 10 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (4 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 10 most recent of 10 reports, in the reporter's own words as published by the FDA.

• InjuryNov 27, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  INCISION & DRAINAGE OF INFECTED HIP.

  Patient problems: Unspecified Infection; Wound Dehiscence

  MAUDE report 20792212 ↗
• InjuryJul 3, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated

  PATIENT REPORTED PAIN AND 2 DISLOCATIONS AND CLOSED REDUCTIONS SINCE REVISION SURGERY. UPDATE: PATIENT HAD A REVISION DUE TO DISLOCATION ON (B)(6) 2022 & ON (B)(6) 2023. THIS PI IS FOR REVISION ON (B)(6) 2023.

  Patient problems: Joint Dislocation; Pain

  MAUDE report 17245220 ↗
• InjuryJun 16, 2023Unstable; Unstable

  AS REPORTED: "DR. PERFORMED A RIGHT HIP REVISION DUE TO INSTABILITY. NO MORE INFORMATION IS AVAILABLE PER DOCTOR."

  Patient problems: Joint Laxity

  MAUDE report 17141218 ↗
• InjuryJan 4, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PROCEDURE: PATIENT UNDERWENT INDEX THA ON (B)(6) 2020. THEN THE PATIENT HAD A PERIPROSTHETIC JOINT INFECTION, SO ALL COMPONENTS WHERE EXCHANGED IN A ONE STAGE REVISION ON (B)(6) 2020.

  Patient problems: Unspecified Infection

  MAUDE report 11108413 ↗
• InjuryOct 26, 2020Insufficient Device Problem Information; Insufficient Device Problem Information

  THIS PI IS FOR PAIN AFTER REVISION. I HAD THA REVISION SURGERY ON (B)(6) 2018. THE STEM WAS REPLACED WITH A STRYKER RESTORATION MODULAR ONE. THE 28 MM CERAMIC FEMORAL HEAD WAS REPLACED WITH A COCR HEAD. HIP, GROIN, AND THIGH PAIN CONTINUED. ON (B)(6) 2019, I WAS DIAGNOSED WITH A STRESS FRACTURE AT THE TIP OF THE PROSTHETIC STEM. ON (B)(6) 2020, I HAD A BONE GRAFT TO REPAIR THE FRACTURE. A CLOUDY MILKY YELLOW FLUID ALONG WITH METAL DEBRIS WAS DISCOVERED IN THE HIP JOINT. ALSO, THERE WAS OSTEOLYSIS IN THE PROXIMAL FEMORAL FEMUR. THE ACETABULAR HAD OVERHANGING SCAR TISSUE AND BONE. THE TRUNNION HAD STRIPE WEAR INDICATING IMPINGEMENT AND LIKELY SOURCE OF THE METALLOSIS. THE 28 MM FEMORAL HEAD WAS REPLACED WITH A 40MM COCR HEAD. SYMPTOMS OF METALLOSIS CONTINUE. FDA SAFETY REPORT ID# (B)(4). UPDATE: AS PER THE PATIENT, HE HAD A LEFT THA ON (B)(6) 2016. HE STARTED TO EXPERIENCE PAIN AT THE END OF (B)(6) 2016. THE PATIENT HAD A BONE SCAN DON ON (B)(6) 2017 (APPROX.) WHICH INDICATED INFECTION/IMPLANT LOOSENING. NO TREATMENT WAS GIVEN TO THE PATIENT. ON (B)(6) 2017 (APPROX.) HE WAS PLACED ON ORAL ANTIBIOTICS FOR 30 DAYS DUE TO INFECTION. ON (B)(6) 2017 X-RAYS CONFIRMED LOOSENING AND THE PATI

  Patient problems: Pain

  MAUDE report 10738216 ↗
• InjuryFeb 25, 2020Material Erosion; Material Erosion

  IT WAS REPORTED THAT THE PATIENT'S RIGHT HIP WAS REVISED. AS REPORTED BY REP: "CLICKING/ UNSTABLE." REP PROVIDED THE PRIMARY OPERATIVE REPORT AND IMPLANT REPORT, AND PICTURES OF THE EXPLANTS SHOWING DAMAGE TO THE REVISED STEM, HEAD, AND LINER. REP REPORTED THAT NO FURTHER INFORMATION IS AVAILABLE.

  Patient problems: Injury

  MAUDE report 9750250 ↗
• InjurySep 3, 2019Device Dislodged or Dislocated; Device Dislodged or Dislocated

  PATIENT HAD A FEW DISLOCATIONS AND DOCTOR WAS ABLE TO CLOSE REDUCE IT WITHOUT INFORMING THE REP. PHYSICIAN DECIDED TO CHANGE TO DUAL MOBILITY FOR BETTER STABILITY.

  Patient problems: Injury; Joint Dislocation

  MAUDE report 8955407 ↗
• InjuryJul 16, 2019Insufficient Device Problem Information; Insufficient Device Problem Information

  PATIENT WAS ADMITTED TO ER DUE TO DRAINAGE OF THE HIP AT INCISION SITE OF PRIOR TOTAL HIP REPLACEMENT. SYMPTOMS OUTSIDE OF DRAINAGE UNKNOWN. THE ON-CALL DOCTOR REVIEWED THE PATIENT'S CONDITION AND AFTER FLUID TESTS WERE RUN, IT WAS DEEMED THE PATIENT'S HIP WAS POTENTIALLY INFECTED. THE PATIENT WAS THEN SCHEDULED FOR SURGERY TO REMOVE THE IMPLANTS AND PLACE A CEMENTED ANTIBIOTIC SPACER. THE REVISION SURGERY THEN TOOK PLACE ON (B)(6) 2019, WHERE THE IMPLANTS WERE REMOVED, FLUID AND TISSUE SENT FOR TESTING, AND FOLLOWING POSITIVE RESULTS OF INFECTION, A CEMENTED ANTIBIOTIC SPACER WAS IMPLANTED. NO FURTHER INFORMATION IS AVAILABLE.

  Patient problems: Injury; Unspecified Infection

  MAUDE report 8793814 ↗
• InjuryJun 18, 2018Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT PATIENT'S LEFT HIP WAS REVISED AFTER REPORTEDLY EXPERIENCING TWO DISLOCATIONS (DATES UNKNOWN). PATIENT WAS REVISED TO AN ADM/MDM LINER CONSTRUCT AND AN UNKNOWN HEAD.

  Patient problems: Injury; Joint Dislocation

  MAUDE report 7609471 ↗
• InjuryApr 18, 2018Device Dislodged or Dislocated; Device Dislodged or Dislocated

  PATIENT PRESENTED WITH DISLOCATED HIP. REVISION SURGERY WAS DONE.

  Patient problems: Injury; Joint Dislocation

  MAUDE report 7441846 ↗