Continuum® Trilogy® Allofit® Longevity® 00-8752-010-36Recalls & reported problems

Summary

The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 00889024149724), received between Aug 27, 2021 and May 15, 2025 — classified as 3 injuries, 5 malfunctions.

The most frequently reported specific device problem is “Difficult to Insert” (3 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.

• MalfunctionMay 15, 2025Difficult to Insert; Difficult to Insert

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

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22026365 ↗
• MalfunctionJul 17, 2024Packaging Problem; Packaging Problem

  IT WAS REPORTED THAT WHEN THE PACKAGE WAS OPENED A HAIR WAS NOTED INSIDE THE LINER.THE EVENT HAPPENED DURING AN INITIAL SURGERY. SURGICAL TECHNIQUE WAS UTILIZED. THERE WAS NO PATIENT IMPACT. THERE WAS NO MEDICAL OR SURGICAL INTERVENTION. THERE WAS NO SURGICAL DELAY AND NO SURGICAL COMPLICATIONS. FOREIGN BODY WAS NOT RETAINED. NO ADDITIONAL INFORMATION AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19766644 ↗
• InjuryApr 24, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED PATIENT UNDERWENT A REVISION PROCEDURE FOUR YEARS POST IMPLANTATION DUE TO UNKNOWN REASON. NO MORE INFORMATION IS AVAILABLE.

  Patient problems: Insufficient Information

  MAUDE report 19175385 ↗
• InjuryJan 3, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED PATIENT UNDERWENT A REVISION PROCEDURE FOUR YEARS POST IMPLANTATION DUE TO UNKNOWN REASON. NO MORE INFORMATION IS AVAILABLE.

  Patient problems: Insufficient Information

  MAUDE report 18438437 ↗
• MalfunctionNov 3, 2023Fracture; Difficult to Insert; Material Twisted/Bent; Fracture; Difficult to Insert; Material Twisted/Bent

  IT WAS REPORTED THAT DURING THE PROCEDURE WHILE TRYING TO REDUCE THE HEAD INTO THE ACETABULUM, THE RIM OF THE POLY LINER BENT INWARD AND MADE IT DIFFICULT FOR THE HEAD TO FULLY ASSEMBLE. ANOTHER LINER AND HEAD WERE USED TO COMPLETE THE PROCEDURE. THERE WAS NO HARM OR HEALTH IMPACT TO THE PATIENT. IT WAS REPORTED THAT NO FURTHER INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18066376 ↗
• MalfunctionOct 5, 2023Difficult to Insert; Difficult to Insert

  NO ADDITIONAL EVENT INFORMATION TO REPORT AT THIS TIME.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17878498 ↗
• MalfunctionMay 5, 2022Positioning Failure; Positioning Failure

  IT WAS REPORTED THAT AN ACETABULUM 52 WAS OPENED, AND AT THE TIME OF PLACING LINER 36, IT DID NOT FIX INSIDE THE ACETABULUM, SO A NEW LINER 32 WAS OPENED BECAUSE THE MEDICAL TEAM THOUGHT THAT LINER 36 WAS DEFECTIVE. WHEN THEY USED THE LINER 32, IT DIDN'T FIX IT IN THE ACETABULUM EITHER. THE DOCTOR TOOK OUT THE 52 ACETABULUM AND TESTED BOTH LINERS OUTSIDE THE PATIENT, AND NEITHER ONE OF THEM FIXED INSIDE THE ACETABULUM. THEY HAD TO OPEN THE 54 ACETABULUM AND THE 36 LINER TO FINISH THE SURGERY. NO ADVERSE EVENTS HAVE BEEN REPORTED AS A RESULT OF THE MALFUNCTION. 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 14287549 ↗
• InjuryAug 27, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED IN A JOURNAL ARTICLE THAT THE PATIENT UNDERWENT A REVISION PROCEDURE OF THE RIGHT HIP DUE TO THE DEVELOPMENT OF A HEMATOMA REQUIRING SURGICAL EVACUATION. NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Hematoma

  MAUDE report 12376995 ↗