Continuum® Trilogy® Allofit® Longevity® 00-8752-012-36Recalls & reported problems

Summary

The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 00889024149786), received between Aug 30, 2019 and Jan 5, 2026 — classified as 4 injuries, 4 malfunctions.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (2 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.

• MalfunctionJan 5, 2026Difficult to Insert

  IT WAS REPORTED THAT THE LINER WOULD NOT LOCK IN THE CUP. 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 23960359 ↗
• InjurySep 19, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  NO ADDITIONAL INFORMATION AVAILABLE FOR THE REPORTED EVENT.

  Patient problems: Ambulation or Postural Difficulties; Deformity/ Disfigurement; Fever; Hypersensitivity/Allergic reaction; Itching Sensation; Loss of Range of Motion; Nerve Damage; Neuropathy; Pain; Skin Discoloration; Swelling/ Edema; Unequal Limb Length

  MAUDE report 23094541 ↗
• InjuryAug 18, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THE PATIENT WAS IMPLANTED WITH ZIMMER BIOMET DEVICES. SUBSEQUENTLY, THE PATIENT WAS REVISED SEVEN YEARS POST IMPLANTATION DUE TO DISLOCATION. THE HEAD AND LINER WERE EXCHANGED.

  Patient problems: Joint Dislocation

  MAUDE report 17574275 ↗
• InjuryOct 13, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT AFTER THE END OF THE SURGERY, WITH THE PATIENT ALREADY SUTURED, THE DOCTOR PERFORMED MOVEMENTS TO EVALUATE THE HIP JOINT WHEN THE PROSTHESIS FAILED. HIP PROSTHESIS DISLOCATED AND THE PATIENT WAS IMMEDIATELY REVISED WHILE STILL UNDER ANESTHESIA. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

  Patient problems: Joint Dislocation

  MAUDE report 15594320 ↗
• MalfunctionApr 12, 2022Fracture; Fracture

  IT WAS REPORTED THAT DURING AN INITIAL HIP ARTHROPLASTY, THE LINER WAS FOUND TO BE FRACTURED. 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 14084660 ↗
• InjuryDec 20, 2019Detachment of Device or Device Component; Detachment of Device or Device Component

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

  Patient problems: No Code Available

  MAUDE report 9503420 ↗
• MalfunctionNov 21, 2019Positioning Failure; Positioning Failure

  NO ADDITIONAL EVENT INFORMATION TO REPORT AT THIS TIME.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9353784 ↗
• MalfunctionAug 30, 2019Tear, Rip or Hole in Device Packaging; Tear, Rip or Hole in Device Packaging

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

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8949365 ↗