Trilogy® Longevity® 00-6334-050-28 (UDI 00889024126084)Recalls & reported problems

Summary

The FDA's MAUDE database contains 11 adverse event reports that list this exact device (DI 00889024126084), received between Oct 30, 2019 and Sep 30, 2026 — classified as 11 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (7 reports).

1 other recall cover devices cleared under the same FDA submission (K071718, K972774); they may or may not involve this specific model.

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 11 most recent of 11 reports, in the reporter's own words as published by the FDA.

• InjurySep 30, 2026Device Dislodged or Dislocated

  It was reported that the patient underwent an initial left hip arthroplasty. The patient fell and experienced a dislocation which was reduced in the ER. Subsequently, a revision procedure was performed approximately 4 years post-implantation due to chronic dislocation. It was reported that no further information is available.

  Patient problems: Fall; Joint Dislocation

  MAUDE report 50945038 ↗
• InjuryApr 27, 2026Device Dislodged or Dislocated

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A HIP REVISION APPROXIMATELY 5-YEARS POST-IMPLANTATION DUE TO DISLOCATION. NO PATIENT HARM OR IMPACT REPORTED DURING THE PROCEDURE. IT WAS CONFIRMED THAT NO FURTHER INFORMATION COULD BE PROVIDED.

  Patient problems: Joint Dislocation

  MAUDE report 25002050 ↗
• InjuryNov 19, 2025Unstable; Unstable

  NO FURTHER INFORMATION AT THE TIME OF THIS REPORT.

  Patient problems: Joint Laxity

  MAUDE report 23594736 ↗
• InjuryFeb 5, 2025Detachment of Device or Device Component; Adverse Event Without Identified Device or Use Problem; Detachment of Device or Device Component; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A REVISION PROCEDURE 5 YEARS AND 2 MONTHS POST IMPLANTATION DUE TO INSTABILITY FROM THE CONSTRAINED LINER FAILURE AND RING DISASSOCIATION IN WHICH THE HEAD AND LINER WERE REVISED. THERE IS NO FURTHER INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Failure of Implant; Insufficient Information; Joint Dislocation

  MAUDE report 21313158 ↗
• InjuryNov 21, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A REVISION PROCEDURE 68 DAYS POST IMPLANTATION DUE TO RECURRENT DISLOCATIONS. HEAD, LINER AND CUP WERE EXCHANGED AND A 30MM SEGMENT WAS ADDED TO THE PROXIMAL FEMUR TO MAKE IT MORE STABLE. THERE IS NO ADDITIONAL INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Joint Dislocation

  MAUDE report 20750835 ↗
• InjuryJul 1, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A REVISION PROCEDURE 1 YEAR AND 9 MONTHS POST IMPLANTATION DUE TO A DISLOCATION AT THE SITE. THERE IS NO ADDITIONAL INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Joint Dislocation

  MAUDE report 19644671 ↗
• InjuryMay 21, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL HIP PROCEDURE ON AN UNKNOWN DATE. SUBSEQUENTLY, THE PATIENT UNDERWENT A REVISION DUE TO DISLOCATION. IT WAS REPORTED THAT NO FURTHER INFORMATION IS AVAILABLE.

  Patient problems: Joint Dislocation

  MAUDE report 19357769 ↗
• InjuryDec 20, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated

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

  Patient problems: Joint Dislocation

  MAUDE report 18363317 ↗
• InjuryApr 28, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED PATIENT UNDERWENT A RIGHT HIP REVISION DUE TO DISLOCATION. DURING THE PROCEDURE THE SURGEON REPLACED THE LINER. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

  Patient problems: Joint Dislocation

  MAUDE report 14238911 ↗
• InjuryOct 30, 2019Corroded; Corroded

  UPON RECEIPT OF ADDITIONAL INFORMATION, IT WAS DETERMINED THIS PRODUCT SHOULD NOT HAVE BEEN REPORTED UNDER THIS MFR NUMBER. THIS REPORT SHOULD BE VOIDED AND A CORRECTED REPORT WILL BE FILED UNDER MFR NUMBER (B)(4).

  Patient problems: Limited Mobility Of The Implanted Joint; Tissue Damage

  MAUDE report 9255661 ↗
• InjuryOct 30, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

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

  Patient problems: Limited Mobility Of The Implanted Joint; Tissue Damage

  MAUDE report 9255209 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K071718, K972774. One submission often covers many models, so check the product and lot details in each record.

• Z-0386-2013 · Aug 27, 2012 · Terminated
  Trilogy II Constrained Liner The Trilogy Longevity Constrained Liner serves as the articular surface for a femoral head in total hip arthroplasty.