Continuum Trilogy Allofit LongevityRecalls & reported problems across all models
Zimmer, Inc. · 39 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 122
- Deaths reported
- 0
- Injuries reported
- 63
- Recalls
- 0
We found 39 models of Continuum Trilogy Allofit Longevity by Zimmer, Inc. in the FDA's device registry (GUDID). Together they are named in 122 adverse event reports in the FDA's MAUDE database, received between Aug 30, 2019 and Jun 1, 2026 — classified as 63 injuries, 59 malfunctions.
The most frequently reported specific device problem is “Difficult to Insert” (42 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported Continuum Trilogy Allofit Longevity problems
Device problems
- Difficult to Insert42
- Device Dislodged or Dislocated37
- Adverse Event Without Identified Device or Use Problem13
- Positioning Failure10
- Fracture8
- Packaging Problem4
- Manufacturing, Packaging or Shipping Problem3
- Malposition of Device2
Patient problems
- No Clinical Signs, Symptoms or Conditions54
- Joint Dislocation35
- Pain15
- Failure of Implant10
- Ambulation or Postural Difficulties4
- Insufficient Information4
- Metal Related Pathology4
- No Known Impact Or Consequence To Patient4
Continuum Trilogy Allofit Longevity models
39 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Continuum® Trilogy® Allofit® Longevity® 00-8752-008-32Prosthesis, hip, semi-constrained, metal/polymer, cemented15 reports
- Continuum® Trilogy® Allofit® Longevity® 00-8751-010-36Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented8 reports
- Continuum® Trilogy® Allofit® Longevity® 00-8752-009-32Prosthesis, hip, semi-constrained, metal/polymer, cemented8 reports
- Continuum® Trilogy® Allofit® Longevity® 00-8752-010-36Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented8 reports
- Continuum® Trilogy® Allofit® Longevity® 00-8752-012-36Prosthesis, hip, semi-constrained, metal/polymer, cemented8 reports
- Continuum® Trilogy® Allofit® Longevity® 00-8752-010-32PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED7 reports
- Continuum® Trilogy® Allofit® Longevity® 00-8751-009-32PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED4 reports
- Continuum® Trilogy® Allofit® Longevity® 00-8751-011-36Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented4 reports
- Continuum® Trilogy® Allofit® Longevity® 00-8751-013-36Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented4 reports
- Continuum® Trilogy® Allofit® Longevity® 00-8752-007-28Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented4 reports
- Continuum® Trilogy® Allofit® Longevity® 00-8758-009-28Prosthesis, hip, constrained, cemented or uncemented, metal/polymer4 reports
- Continuum® Trilogy® Allofit® Longevity® 00-8758-011-28Prosthesis, hip, constrained, cemented or uncemented, metal/polymer4 reports
- Continuum® Trilogy® Allofit® Longevity® 00-8751-008-32Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented3 reports
- Continuum® Trilogy® Allofit® Longevity® 00-8752-013-36Prosthesis, hip, semi-constrained, metal/polymer, cemented3 reports
- Continuum® Trilogy® Allofit® Longevity® 00-8752-014-32Prosthesis, hip, semi-constrained, metal/polymer, cemented3 reports
- Continuum® Trilogy® Allofit® Longevity® 00-8752-014-36Prosthesis, hip, semi-constrained, metal/polymer, cemented3 reports
- Continuum® Trilogy® Allofit® Longevity® 00-8751-012-36PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 reports
- Continuum® Trilogy® Allofit® Longevity® 00-8752-005-22Prosthesis, hip, semi-constrained, metal/polymer, cemented2 reports
- Continuum® Trilogy® Allofit® Longevity® 00-8752-006-28PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 reports
- Continuum® Trilogy® Allofit® Longevity® 00-8752-011-36Prosthesis, hip, semi-constrained, metal/polymer, cemented2 reports
- Continuum® Trilogy® Allofit® Longevity® 00-8752-012-32Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented2 reports
- Continuum® Trilogy® Allofit® Longevity® 00-8752-013-32PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 reports
- Continuum® Trilogy® Allofit® Longevity® 00-8755-010-36Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented2 reports
- Continuum® Trilogy® Allofit® Longevity® 00-8758-012-32Prosthesis, hip, constrained, cemented or uncemented, metal/polymer2 reports
- Continuum® Trilogy® Allofit® Longevity® 00-8758-013-32Prosthesis, hip, constrained, cemented or uncemented, metal/polymer2 reports
- Continuum® Trilogy® Allofit® Longevity® 00-8751-007-28PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- Continuum® Trilogy® Allofit® Longevity® 00-8751-010-32PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- Continuum® Trilogy® Allofit® Longevity® 00-8751-012-32Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- Continuum® Trilogy® Allofit® Longevity® 00-8751-012-40PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- Continuum® Trilogy® Allofit® Longevity® 00-8751-013-40Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- Continuum® Trilogy® Allofit® Longevity® 00-8751-014-36Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- Continuum® Trilogy® Allofit® Longevity® 00-8751-015-36PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- Continuum® Trilogy® Allofit® Longevity® 00-8752-015-36Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- Continuum® Trilogy® Allofit® Longevity® 00-8752-018-32Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- Continuum® Trilogy® Allofit® Longevity® 00-8754-009-32Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- Continuum® Trilogy® Allofit® Longevity® 00-8754-016-32Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- Continuum® Trilogy® Allofit® Longevity® 00-8758-010-28Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 report
- Continuum® Trilogy® Allofit® Longevity® 00-8758-012-28Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 report
- Continuum® Trilogy® Allofit® Longevity® 00-8758-014-36Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 report
Recent Continuum Trilogy Allofit Longevity adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryJun 1, 2026Device Dislodged or Dislocated
IT WAS REPORTED THAT APPROXIMATELY EIGHT MONTHS POST-TOTAL FEMORAL HIP REPLACEMENT, THE PATIENT UNDERWENT A HIP REVISION DUE TO DISLOCATION. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Joint Dislocation
MAUDE report 25347831 ↗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 ↗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 ↗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 ↗InjuryOct 21, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated
IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL HIP ARTHROPLASTY AND WAS IMPLANTED WITH ZIMMER BIOMET AND COMPETITOR PRODUCTS. SUBSEQUENTLY, THE PATIENT WAS REVISED EIGHT (8) YEARS POST IMPLANTATION DUE TO DISLOCATION. THE LINER, SHELL, AND SCREWS WERE EXPLANTED.
Patient problems: Joint Dislocation
MAUDE report 23350755 ↗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 ↗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 22963957 ↗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 ↗InjurySep 3, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT APPROXIMATELY EIGHT YEARS POST-IMPLANTATION, THE PATIENT UNDERWENT A HIP REVISION DUE TO PAIN AND DIFFICULTIES WITH ADLS. ALL COMPONENTS WERE REVISED. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Pain
MAUDE report 22955087 ↗InjuryAug 11, 2025Fracture; Fracture
NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Insufficient Information
MAUDE report 22778910 ↗MalfunctionJul 16, 2025Difficult to Insert; Difficult to Insert
IT WAS REPORTED THAT DURING SURGERY, IT WAS DIFFICULT TO IMPLANT THE LINER INTO THE CUP, WHICH LED TO POOR STABILITY OF THE CUP. THE CUP REMAINED LOOSE. A NEW CUP WAS IMPLANTED AND THE SAME LINER WAS ABLE TO BE USED. THERE WAS A FIVE-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 22527229 ↗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 ↗InjuryJun 6, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT APPROXIMATELY EIGHT YEARS POST-IMPLANTATION, THE PATIENT UNDERWENT A HIP REVISION DUE TO PAIN AND DIFFICULTIES WITH ADLS. ALL COMPONENTS WERE REVISED. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Pain
MAUDE report 22157344 ↗MalfunctionMay 15, 2025Difficult to Insert; Difficult to Insert
IT WAS REPORTED THAT THE LINER WOULD NOT MATE WITH THE CUP. A NEW LINER WAS OPENED AND SUCCESSFULLY IMPLANTED WITH 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 22026611 ↗
Other Zimmer, Inc. products
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- Persona The Personalized Knee77 models · 1,396 reports
- PERSONA Vivacit-E285 models · 1,152 reports
- NexGen198 models · 842 reports · 4 recalls
- Affixus18 models · 1 reports · 17 recalls
- PERSONA Natural Tibia25 models · 417 reports · 2 recalls
- NexGen Legacy119 models · 319 reports · 3 recalls
- Alliance32 models · 275 reports · 2 recalls
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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