Trilogy LongevityRecalls & reported problems across all models
Zimmer, Inc. · 29 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 123
- Deaths reported
- 0
- Injuries reported
- 114
- Recalls
- 0
We found 29 models of Trilogy Longevity by Zimmer, Inc. in the FDA's device registry (GUDID). Together they are named in 123 adverse event reports in the FDA's MAUDE database, received between Oct 30, 2019 and Sep 30, 2026 — classified as 114 injuries, 9 malfunctions.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (65 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 Trilogy Longevity problems
Device problems
- Device Dislodged or Dislocated65
- Adverse Event Without Identified Device or Use Problem29
- Fracture13
- Difficult to Insert9
- Naturally Worn9
- Unstable6
- Insufficient Device Problem Information5
- Material Erosion3
Patient problems
- Joint Dislocation67
- Pain25
- Failure of Implant14
- Insufficient Information14
- Muscle/Tendon Damage10
- No Clinical Signs, Symptoms or Conditions10
- Metal Related Pathology7
- Fall5
Trilogy Longevity models
29 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Trilogy® Longevity® 6305-50-36PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED36 reports
- Trilogy® Longevity® 6310-50-32PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED15 reports
- Trilogy® Longevity® 00-6334-050-28PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED11 reports
- Trilogy® Longevity® 6305-50-32PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED10 reports
- Trilogy® Longevity® 6305-56-36PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED6 reports
- Trilogy® Longevity® 6310-58-36PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED6 reports
- Trilogy® Longevity® 6310-56-32PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED5 reports
- Trilogy® Longevity® 6310-48-32PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED4 reports
- Trilogy® Longevity® 6320-48-32PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED3 reports
- Trilogy® Longevity® 6305-58-36PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 reports
- Trilogy® Longevity® 6305-60-36PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 reports
- Trilogy® Longevity® 6310-60-36PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 reports
- Trilogy® Longevity® 6310-62-36PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 reports
- Trilogy® Longevity® 6320-50-32PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 reports
- Trilogy® Longevity® 6320-56-32PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 reports
- Trilogy® Longevity® 00-6334-050-28Prosthesis, hip, constrained, cemented or uncemented, metal/polymer2 reports
- Trilogy® Longevity® 6305-48-32PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- Trilogy® Longevity® 6305-56-32PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- Trilogy® Longevity® 6305-58-28PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- Trilogy® Longevity® 6305-58-40PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- Trilogy® Longevity® 6305-62-40PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- Trilogy® Longevity® 6310-46-22PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- Trilogy® Longevity® 6310-62-32PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- Trilogy® Longevity® 6320-58-32PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- Trilogy® Longevity® 00-6334-058-32PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- Trilogy® Longevity® 6341-50-32PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- Trilogy® Longevity® 6305-56-36PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- Trilogy® Longevity® 6310-48-32PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- Trilogy® Longevity® 6310-56-32PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
Recent Trilogy Longevity adverse event reports
The 15 most recent reports across all models, 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 ↗InjuryJun 14, 2026Device Dislodged or Dislocated
No further information is available at the time of this report.
Patient problems: Joint Dislocation
MAUDE report 25497535 ↗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 ↗InjuryMar 24, 2026Fracture; Naturally Worn; Noise, Audible
IT WAS REPORTED THAT APPROXIMATELY THREE YEARS POST-IMPLANTATION, THE PATIENT UNDERWENT A RIGHT HIP REVISION DUE TO REPORTED NOISES AND PREMATURE POLY WEAR AND THE POLY WAS BROKEN. THE PATIENT REPORTED SQUEAKING DURING WALKING AND MOBILIZATION WITHOUT PAINFUL SYMPTOMS, WHICH LIMITED DAILY ACTIVITIES. THE REVISION WAS PERFORMED AND THERE WAS PREMATURE WEAR OF THE POLYETHYLENE. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Insufficient Information
MAUDE report 24680737 ↗InjuryMar 16, 2026Device Dislodged or Dislocated
IT WAS REPORTED THAT APPROXIMATELY SEVEN WEEKS POST-IMPLANTATION, THE PATIENT UNDERWENT A HIP REVISION DUE TO EXPERIENCING SEVERAL DISLOCATIONS. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Joint Dislocation
MAUDE report 24606424 ↗InjuryFeb 5, 2026Device Dislodged or Dislocated
IT WAS REPORTED THAT THE PATIENT EXPERIENCED A CLOSED REDUCTION AND IS PENDING A LEFT HIP REVISION WITH A TRIFLANGE DUE TO DISLOCATION, OSTEOLYSIS, AND NON-DISPLACED SUPERIOR AND INFERIOR PUBIC RAMI FRACTURES. THE PATIENT HAS SOME INSTABILITY AND THE LOCKING MECHANISM FOR COMPONENTS APPARENTLY FAILED. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Bone Fracture(s); Joint Dislocation; Osteolysis
MAUDE report 24267988 ↗InjuryJan 13, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT APPROXIMATELY NINE MONTHS POST-HIP SURGERY, THE PATIENT UNDERWENT A RIGHT HIP REVISION DUE TO GREATER TROCHANTER FRACTURE AND ABDUCTOR DEFICIENCY, A LARGE TEAR WAS NOTED. DURING THE PROCEDURE, THERE WAS TRUNNIONOSIS ON THE STEM TRUNNION. THE CUP AND STEM WERE RETAINED AND A CONSTRAINED LINER PLACED. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Bone Fracture(s); Metal Related Pathology; Muscle/Tendon Damage
MAUDE report 24052224 ↗MalfunctionDec 16, 2025Device Contaminated During Manufacture or Shipping; Device Contaminated During Manufacture or Shipping
IT WAS REPORTED THAT WHEN OPENING THE IMPLANT, BLACK DEBRIS WAS DETECTED ON THE BACK OF THE LINER. A NEW LINER WAS USED INSTEAD TO AVOID IMPLANTING THE ONE WITH THE DEBRIS. 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 23821108 ↗InjuryNov 19, 2025Unstable; Unstable
NO FURTHER INFORMATION AT THE TIME OF THIS REPORT.
Patient problems: Joint Laxity
MAUDE report 23594736 ↗InjuryNov 17, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
NO ADDITIONAL EVENT INFORMATION.
Patient problems: Loss of Range of Motion; Pain; Unequal Limb Length
MAUDE report 23569214 ↗InjuryNov 13, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated
IT WAS REPORTED THAT THE PATIENT UNDERWENT A HIP REVISION DUE TO RECURRENT DISLOCATION AND CUP LOOSENING. THE G7 OSSEOTI MULTI HOLE WAS REPLACED WITH A DUAL MOBILITY. IT WAS CONFIRMED THAT NO FURTHER INFORMATION COULD BE PROVIDED.
Patient problems: Aseptic loosening; Joint Dislocation
MAUDE report 23542042 ↗InjuryNov 7, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated
IT WAS REPORTED THAT THE PATIENT UNDERWENT A HIP REVISION APPROXIMATELY 5 YEARS AND 5 MONTHS POST-IMPLANTATION DUE TO DISLOCATION. THE HEAD AND LINER WERE EXPLANTED. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Joint Dislocation
MAUDE report 23497955 ↗InjurySep 16, 2025Off-Label Use; Device Dislodged or Dislocated; Off-Label Use; Device Dislodged or Dislocated
NO ADDITIONAL INFORMATION AVAILABLE FOR THE REPORTED EVENT.
Patient problems: Joint Dislocation
MAUDE report 23061624 ↗MalfunctionSep 2, 2025Difficult to Insert; Difficult to Insert
NO FURTHER INFORMATION AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22937315 ↗MalfunctionAug 14, 2025Difficult to Insert; Difficult to Insert
NO FURTHER INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22809625 ↗
Other Zimmer, Inc. products
- PERSONA364 models · 2,000 reports · 3 recalls
- 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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