Trident X3 Insert 723-10-32ERecalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 07613327339109), received between Mar 22, 2023 and Sep 21, 2026 — classified as 4 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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 16, 2026.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• InjurySep 21, 2026Use of Device Problem

  Patient problems: Wound Dehiscence

  MAUDE report 50845448 ↗
• InjuryJul 22, 2024Device-Device Incompatibility; Device Dislodged or Dislocated; Device-Device Incompatibility; Device Dislodged or Dislocated

  PATIENT DIAGNOSED WITH OSTEONECROSIS OF THE FEMORAL HEAD OF THE LEFT HIP, WHO UNDERWENT UNCEMENTED TOTAL ARTHROPLASTY OF THE LEFT HIP WITH A CERAMIC-POLYETHYLENE TRIBOLOGICAL PAIR ON (B)(6) 2024. DURING THE UNEVENTFUL PROCEDURE, SATISFACTORY STABILITY TESTS WERE CARRIED OUT. A 50MM ACETABULAR COMPONENT AND 36MM FEMORAL HEAD WERE USED. AFTER A CONTROL RADIOGRAPHY, THE IMAGE DREW ATTENTION TO THE SUBLUXATION OF THE FEMORAL HEAD IN RELATION TO THE ACETABULAR COMPONENT. DUE TO SUSPICION OF LOOSENING OF THE POLYETHYLENE LINER OR INTERPOSITION OF SOFT TISSUES, A SURGICAL REVIEW WAS INDICATED THE FOLLOWING DAY (B)(6) 2024 AND THE PATIENT'S HOSPITALIZATION WAS EXTENDED. DURING THE NEW SURGERY, IT WAS FOUND THAT THE POLYETHYLENE LINER WAS PERFECTLY LOCKED, BUT THE 36 MM HEAD WAS NOT FULLY FITTED. THE POLYETHYLENE LINER WAS REMOVED AND THE ENGRAVING ON THE PIECE WAS CHECKED, WHICH CONFIRMED THAT THE INTERNAL DIAMETER WAS ACTUALLY 32 MM, CONTRARY TO WHAT WAS FOUND IN THE PREVIOUS DAY'S SURGERY. THE LINER WAS REPLACED WITH A 36MM INTERNAL DIAMETER COMPONENT AND THERE WAS A GOOD REDUCTION. THE PATIENT WAS DISCHARGED FROM HOSPITAL THE FOLLOWING DAY, 06/22/2024. THE PRODUCT BOX WAS NOT STORED BEC

  Patient problems: Joint Dislocation

  MAUDE report 19800388 ↗
• InjuryFeb 29, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT RETURNED TO THEATRE FOR A HEAD LINER EXCHANGE DUE TO INFECTION STRYKER TRITANIUM 2 SHELL AND LINE DEPUY CORAIL STEM AND HEAD.

  Patient problems: Unspecified Infection

  MAUDE report 18806108 ↗
• InjuryMar 22, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT REQUIRED A HIP REVISION FOR INFECTION, 1ST STAGE HIP REVISION. REMOVING AN EXETER V40 STEM, TRIDENT HEMISPHERICAL ACETABULAR SHELL SIZE 52 ,SMALL ARTISAN CEMENT PLUG. UNSURE IS STILL HAD A TRIDENT X3 10 DEGREE LINER OR CERAMIC V40 32MM HEAD INSITU AS IMPLANT STICKERS SENT FROM SURGEON FOR PATIENT SAID THE PATIENT HAD A CERAMIC V40 HEAD BUT THEN THE REMOVED HEAD APPEARED TO BE METAL AND THE SURGEON SPECIFIED THE PATIENT ALREADY HAD THIS REPLACED BUT UNABLE TO GIVE FURTHER DETAILS. REPLACED WITH A COMPETITOR CUP AND LINER. STRYKER REPLACED WITH LFIT V40 28MM HEAD +4MM AND EXETER LONG STEM 44 NO2 205MM.

  Patient problems: Unspecified Infection

  MAUDE report 16591373 ↗