Trilogy® Longevity® 6310-50-32Recalls & reported problems
Zimmer, Inc. · Class 2 · Implant
- Adverse event reports
- 15
- Deaths reported
- 0
- Injuries reported
- 12
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 15 adverse event reports that list this exact device (DI 00889024124721), received between Jun 16, 2021 and Mar 16, 2026 — classified as 12 injuries, 3 malfunctions.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (8 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Device Dislodged or Dislocated8
- Adverse Event Without Identified Device or Use Problem4
- Difficult to Insert3
- Unintended Movement1
Patient problems
- Joint Dislocation8
- Insufficient Information3
- No Clinical Signs, Symptoms or Conditions3
- Aseptic loosening1
- Failure of Implant1
- Metal Related Pathology1
- Pain1
Recent adverse event reports
The 15 most recent of 15 reports, in the reporter's own words as published by the FDA.
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 ↗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 ↗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 ↗InjuryAug 11, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Joint Dislocation
MAUDE report 22779141 ↗InjuryJul 14, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT APPROXIMATELY 4 AND A HALF YEARS POST-IMPLANTATION, THE PATIENT UNDERWENT A HIP REVISION DUE TO INSTABILITY. THE HEAD AND LINER WERE EXCHANGED. IT WAS REPORTED THAT NO FURTHER INFORMATION IS AVAILABLE.
Patient problems: Insufficient Information
MAUDE report 22492926 ↗InjuryJul 1, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL HIP PROCEDURE. SUBSEQUENTLY, THE PATIENT WAS REVISED APPROXIMATELY TWO YEARS LATER DUE TO A PSOAS CONFLICT. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Insufficient Information
MAUDE report 22369906 ↗InjuryMay 20, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT APPROXIMATELY 4 AND A HALF YEARS POST-IMPLANTATION, THE PATIENT UNDERWENT A HIP REVISION DUE TO INSTABILITY. THE HEAD AND LINER WERE EXCHANGED. IT WAS REPORTED THAT NO FURTHER INFORMATION IS AVAILABLE.
Patient problems: Insufficient Information
MAUDE report 22051934 ↗InjuryAug 12, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated
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 (5648920).
Patient problems: Failure of Implant; Joint Dislocation
MAUDE report 19963304 ↗InjuryDec 29, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated
IT WAS REPORTED THAT THE PATIENT WAS REVISED APPROXIMATELY TWELVE YEARS POST-IMPLANTATION DUE TO A DISLOCATION. DURING THE REVISION SURGERY, THE SURGEON NOTICED TRUNION WEAR AND A PSEUDOTUMOR POSSIBLY DUE TO METAL ION RELEASE. IT WAS REPORTED THAT NO FURTHER INFORMATION IS AVAILABLE.
Patient problems: Joint Dislocation; Metal Related Pathology
MAUDE report 18418145 ↗MalfunctionMay 15, 2023Difficult to Insert; Difficult to Insert
IT WAS REPORTED THAT THE LINER WOULD NOT SEAT. THE SURGEON REAMED FOR A 54MM CUP. THE CUP WAS IMPLANTED WITH ADDITIONAL FIXATION SCREWS. IT WAS ENSURED THAT THE SCREWS WERE NOT RAISED. THERE WAS NO VISIBLE SOFT TISSUE IN THE CUP AND ALIGNED SCALLOPS OF THE CUP WITH THE LINER. THE SURGEON IMPACTED WITH A 32MM IMPACTOR HOWEVER THE LINER STILL WOULD NOT SEAT. THERE WAS A 10-MINUTE DELAY. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16930756 ↗InjuryMar 28, 2023Device Dislodged or Dislocated; Unintended Movement; Device Dislodged or Dislocated; Unintended Movement
IT WAS REPORTED A PATIENT UNDERWENT A CLOSED REDUCTION PROCEDURE TO CORRECT A DISLOCATION. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION IS AVAILABLE.
Patient problems: Joint Dislocation
MAUDE report 16627644 ↗InjuryFeb 16, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated
NO ADDITIONAL EVENT INFORMATION TO REPORT AT THIS TIME.
Patient problems: Joint Dislocation
MAUDE report 16387811 ↗InjuryOct 5, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated
IT WAS REPORTED THAT THE PATIENT UNDERWENT A REVISION PROCEDURE APPROXIMATELY 6 YEARS POST IMPLANTATION DUE TO CHRONIC DISLOCATION. NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Joint Dislocation
MAUDE report 15546630 ↗InjuryJul 6, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT EXPERIENCED PAIN IN THE UPPER SIDE OF THE HIP AND ALLEGED SENSATION OF THE TENDON MOVING WITHIN THE JOINT APPROXIMATELY 11 YEARS POST IMPLANTATION. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.
Patient problems: Pain
MAUDE report 14939093 ↗MalfunctionJun 16, 2021Difficult to Insert; Difficult to Insert
IT WAS REPORTED THAT DURING A HIP PROCEDURE, THE LINER WAS OPENED AND FOUND POLY PROTRUDING AT THE BOTTOM OF THE LINER. THE SURGEON OPENED A NEW DEVICE TO COMPLETE THE SURGERY. THERE WAS APPROXIMATELY 30 MIN OF SURGERY DELAY. 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 12010271 ↗
Other PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED devices
- PINNACLE 1217-25-500Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED735 reports
- NA 1365-52-000Depuy (Ireland) · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED683 reports
- APEX 1246-03-000Depuy (Ireland) · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED3 deaths613 reports
- PINNACLE 1217-20-500Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 deaths590 reports
- PINNACLE 1217-30-500Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 death484 reports
- NA 1365-53-000Depuy (Ireland) · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED404 reports
- PINNACLE ALTRX 1221-36-054Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED388 reports
- PINNACLE ALTRX 1221-32-050Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED386 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.