Trilogy® 6260-18Recalls & reported problems

Summary

The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 00889024120136), received between Jul 28, 2021 and Sep 8, 2026 — classified as 2 injuries, 7 malfunctions.

The most frequently reported specific device problem is “Fracture” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 8, 2026Fracture

  It was reported that the cup positioner broke. There are no known impacts to the patient. It was reported that no further information was available.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50673177 ↗
• MalfunctionDec 17, 2025Fracture; Fracture

  NO FURTHER INFORMATION AT THE TIME OF THIS REPORT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23830586 ↗
• MalfunctionFeb 6, 2025Difficult to Insert; Material Deformation; Difficult to Insert; Material Deformation

  NO ADDITIONAL EVENT INFORMATION TO REPORT AT THIS TIME.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21324207 ↗
• MalfunctionJan 8, 2024Separation Failure; Separation Failure

  ADDITIONAL INFORMATION RECEIVED. IT WAS REPORTED THAT THE THREADS WERE NOT AN ISSUE. THE INNER SPRING WAS ALLOWING THE CUP TO SEAT BACK TOO FAR. NO ADDITIONAL INFORMATION WAS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18467236 ↗
• MalfunctionDec 13, 2023Fracture; Fracture

  IT WAS REPORTED THAT THE SHELL INSERTER FRACTURED DURING IMPACTION OF THE SHELL. THERE WAS NO KNOWN IMPACT OR CONSEQUENCES TO THE PATIENT. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18320930 ↗
• MalfunctionJul 6, 2023Material Deformation; Material Deformation

  IT WAS REPORTED THAT DURING THE PROCEDURE, THE THREADS ON THE CUP INSERTER WERE DAMAGED. THERE WAS NO HARM OR HEALTH CONSEQUENCES TO THE PATIENT. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17265910 ↗
• InjuryApr 18, 2022Positioning Failure; Positioning Failure

  IT WAS REPORTED THAT CUP POSITIONER INSTRUMENT WOULDN¿T THREAD INTO THE ACETABULAR SHELL. COMPARED TO OTHER IMPACTORS OF THE SAME TYPE ON-SITE, THE LENGTH OF THE THREADED PORTION OF THIS INSERTER APPEARS SHORTER (WITH THE SHINY SHELL IMPACTOR CAP ON) WHICH WOULD EXPLAIN WHY IT WOULDN¿T THREAD INTO A SHELL. FOUR MINUTE DELAY IN SURGERY WHILE ANOTHER IMPACTOR WAS OBTAINED. NO ADDITIONAL INFORMATION IS AVAILABLE. NO ADVERSE EVENT TO PATIENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14137175 ↗
• InjuryOct 21, 2021Fracture; Fracture

  IT WAS REPORTED THAT DURING AN INITIAL HIP PROCEDURE THAT DURING IMPACTION OF ACETABULUM THE SHELL COMPONENT INSERTER BROKE. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12672336 ↗
• MalfunctionJul 28, 2021Degraded; Degraded

  NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12239184 ↗