TRIDENT II 709-04-52ERecalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 07613327344011), received between Aug 12, 2020 and May 16, 2025 — classified as 3 injuries.

The most frequently reported specific device problem is “Fracture” (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 18, 2026.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjuryMay 16, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  RIGHT-HIP REVISION. PT. PRESENTED WITH A "SUBSTANTIAL" LIMB-LENGTH DISCREPANCY FOLLOWING THA. DR. OPTED TO REVISE THE ACETABULAR COMPONENT, GOING TO AN MDM CONSTRUCT FOR INCREASED STABILITY BECAUSE OF THE REVISION. NO COMPLAINTS FILED AGAINST THE COMPONENTS THEMSELVES, FEMORAL STEM WAS LEFT IN-SITE, NO FURTHER INFO AVAILABLE.

  Patient problems: Unequal Limb Length

  MAUDE report 22038367 ↗
• InjuryJun 9, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT'S LEFT HIP WAS REVISED DUE TO THE PATIENT TRIPPED AFTER IMPLANTATION AND IMPACTING THE SHELL INTO THE ACETABULUM. A TRIDENT TRITANIUM MULTI HOLE SHELL AND FOUR SCREWS WERE REVISED. ASIDE FROM ATTACHED X-RAY, REP CONFIRMED THAT NO FURTHER INFORMATION WOULD BE RELEASED BY THE HOSPITAL OR SURGEON.

  Patient problems: Hip Fracture

  MAUDE report 11968790 ↗
• InjuryAug 12, 2020Fracture; Fracture

  AS REPORTED: PATIENT CAME TO THE OR WITH A VISIBLY ROTATED ACETABULAR COMPONENT. THE COMPONENT WAS REMOVED AND A NEW ACETABULAR COMPONENT WAS PLACED WITH EXTENSIVE SCREW FIXATION AND MDM BEARING WAS CHOSEN." ANY COMPLICATING CONDITIONS NOTES "INITIAL FRACTURE OF THE MEDIAL WALL OF THE ACETABULUM." UPDATE: "THERE WAS A DEFICIENT MEDIAL WALL PRIOR TO THE INITIAL SURGERY, WHICH WAS REVISED TO A MULTI HOLE SHELL, WHICH WAS THEN REVISED TO ANOTHER MULTI HOLE SHELL. 2 REVISIONS, THIS BEING THE SECOND. INITIAL SURGERY (B)(6) 2018, INITIAL REVISION (B)(6) 2018. NO ALLEGATIONS OR PRODUCT DEFICIENCY. REVISION DUE TO PATIENT CONDITION/POOR BONE QUALITY."

  Patient problems: Bone Fracture(s); Injury

  MAUDE report 10395742 ↗