Continuum® Trilogy® Allofit® Longevity® 00-8752-008-32Recalls & reported problems
Zimmer, Inc. · Class 2 · Implant
All models of Continuum Trilogy Allofit Longevity (39)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 15
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 15 adverse event reports that list this exact device (DI 00889024149670), received between Jan 2, 2020 and Apr 24, 2026 — classified as 4 injuries, 11 malfunctions.
The most frequently reported specific device problem is “Difficult to Insert” (10 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.
Reports received per month
Most reported problems
Device problems
- Difficult to Insert10
- Device Dislodged or Dislocated2
- Fracture2
- Positioning Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions10
- Joint Dislocation2
- Aseptic loosening1
- Failure of Implant1
- Insufficient Information1
- Metal Related Pathology1
- No Code Available1
- Periprosthetic fracture1
Recent adverse event reports
The 15 most recent of 15 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 24, 2026Difficult to Insert
IT WAS REPORTED THE LINER COULD NOT BE IMPLANTED INTO THE CUP PROPERLY AND WAS NOTED TO BE SLIGHTLY LOOSE. A NEW LINER WAS OPENED AND SUCCESSFULLY MATED. THERE WERE NO IMPACTS TO THE PATIENT. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24982683 ↗InjuryDec 23, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated
IT WAS CONFIRMED THAT NO FURTHER INFORMATION COULD BE PROVIDED.
Patient problems: Aseptic loosening; Joint Dislocation; Metal Related Pathology; Periprosthetic fracture; Synovitis
MAUDE report 23879535 ↗InjuryDec 23, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated
IT WAS CONFIRMED THAT NO FURTHER INFORMATION COULD BE PROVIDED.
Patient problems: Joint Dislocation
MAUDE report 23879263 ↗MalfunctionSep 4, 2025Difficult to Insert; Difficult to Insert
IT WAS REPORTED THAT DURING THE PROCEDURE, THE 28 MM LINER COULD NOT BE IMPLANTED INTO THE SIZE FF/46 CUP. AFTER SEVERAL ATTEMPTS, THE LINER WOULD NOT IMPLANT AND THE CUP WAS LOOSENING. THE FIRST CUP WAS REMOVED AND A LARGER CUP IMPLANTED. A 32 MM LINER WAS ATTEMPTED TO BE USED AND WOULD NOT IMPLANT. A CERAMIC LINER WAS ABLE TO BE USED TO COMPLETE THE PROCEDURE. THERE WAS A 30-MINUTE DELAY. 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 22963955 ↗InjuryAug 11, 2025Fracture; Fracture
NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Insufficient Information
MAUDE report 22778910 ↗MalfunctionJun 16, 2025Fracture; Fracture
IT WAS REPORTED THAT THE INLAY OF THE HIP PROSTHESIS HAS FRACTURED. FURTHER DETAILS REGARDING SUBSEQUENT MEDICAL INTERVENTION AND/OR PATIENT IMPACT HAVE NOT BEEN REPORTED. DUE DILIGENCE IS IN PROGRESS FOR THIS EVENT; TO DATE NO ADDITIONAL INFORMATION HAS BEEN PROVIDED.
Patient problems: Failure of Implant
MAUDE report 22211529 ↗MalfunctionJul 3, 2024Difficult to Insert; Difficult to Insert
IT WAS REPORTED THAT THE LINER WOULD NOT LOCK WITH THE CUP PROPERLY CAUSING A FORTY (40) MINUTE DELAY. THE LINER APPEARED TO BE SMALLER COMPARED TO THE BACK UP. THE INITIAL CUP WAS IMPLANTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19671656 ↗MalfunctionJun 13, 2024Difficult to Insert; Difficult to Insert
NO FURTHER INFORMATION AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19527696 ↗MalfunctionMay 22, 2023Positioning Problem; Positioning Problem
NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16976565 ↗MalfunctionMay 9, 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 16897281 ↗MalfunctionApr 6, 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 16689378 ↗MalfunctionApr 6, 2023Difficult to Insert; Difficult to Insert
IT WAS REPORTED THAT DURING A PROCEDURE, THE LINER WOULD NOT ASSEMBLE WITH THE CUP. ANOTHER LINER AND CUP OF THE SAME SIZE WERE USED, BUT ALSO WOULD NOT ASSEMBLE CORRECTLY. THE SURGEON THEN, REAMED THE BONE A SECOND TIME WITH ONE SIZE GREATER THAN ANTICIPATED AND THESE DEVICES WERE ABLE TO FUNCTION PROPERLY AND WERE IMPLANTED. IT WAS REPORTED THAT NO FURTHER INFORMATION IS AVAILABLE AT THIS TIME.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16689355 ↗MalfunctionAug 9, 2022Difficult to Insert; Difficult to Insert
IT WAS REPORTED THE LINER WOULD NOT ASSEMBLE WITH THE CUP. A SECOND LINER WAS USED TO COMPLETE THE SURGERY. THE CUP REMAINS IMPLANTED. 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 15196385 ↗MalfunctionMay 10, 2022Difficult to Insert; Difficult to Insert
IT WAS REPORTED DURING AN INITIAL HIP ARTHROPLASTY THE SURGEON HAD DIFFICULTY MATING THE LINER INTO THE CUP. THE PROCEDURE WAS COMPLETED WITH ORIGINAL LINER AND CUP. 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 14348921 ↗InjuryJan 2, 2020Difficult to Insert; Difficult to Insert
IT WAS REPORTED THAT DURING HIP SURGERY, THE LINER WOULD NOT SEAT INTO THE CUP. AFTER REPEATED ATTEMPTS TO SEAT THE LINER INTO THE CUP, IT WAS FOUND THAT THE CUP HAD BECOME LOOSE. THE 48 MM CUP WAS THEN REMOVED AND REPLACED WITH A 50MM CUP. THE LINER WAS THEN IMPLANTED WITH NO ISSUES. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.
Patient problems: No Code Available
MAUDE report 9537926 ↗
Other Prosthesis, hip, semi-constrained, metal/polymer, cemented devices
- NA 1365-51-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented753 reports
- NA 1365-50-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented412 reports
- ARTICUL/EZE 1365-21-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented1 recall280 reports
- ARTICUL/EZE 1365-11-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented1 death262 reports
- LFIT 6260-9-236Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/polymer, cemented256 reports
- PINNACLE GRIPTION 1217-32-052Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/polymer, cemented2 deaths239 reports
- ELEOS™ 25002111EOnkos Surgical, Inc. · Prosthesis, hip, semi-constrained, metal/polymer, cemented3 deaths230 reports
- Novation 130-36-52Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented2 recalls124 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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