Trilogy® Longevity® 6305-50-32Recalls & reported problems
Zimmer, Inc. · Class 2 · Implant
All models of Trilogy Longevity (29)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 10
- Deaths reported
- 0
- Injuries reported
- 9
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 10 adverse event reports that list this exact device (DI 00889024123755), received between Oct 8, 2020 and Sep 2, 2025 — classified as 9 injuries, 1 malfunction.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (9 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
- Device Dislodged or Dislocated9
- Unstable2
- Difficult to Insert1
- Naturally Worn1
- Unintended Movement1
Patient problems
- Joint Dislocation9
- Muscle/Tendon Damage4
- Pain3
- Scar Tissue2
- Failure of Implant1
- Fall1
- Hematoma1
- Inflammation1
Recent adverse event reports
The 10 most recent of 10 reports, in the reporter's own words as published by the FDA.
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 ↗InjuryFeb 7, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated
IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL HIP PROCEDURE. SUBSEQUENTLY, THE PATIENT WAS REVISED APPROXIMATELY 2 MONTHS LATER DUE TO INSTABILITY AND DISLOCATION. DURING THE REVISION, THE SURGEON NOTED THAT THE POSTERIOR CAPSULE WAS ALREADY TRAUMATICALLY REMOVED, AND THE HIP WAS DISLOCATING IN THE SLEEPING POSITION. THE ACETABULAR COMPONENT WAS WELL-FIXED AND IN APPROPRIATE POSITION. THE FEMORAL COMPONENT WAS FOUND LACKING ANTEVERSION BUT WAS WELL-FIXED. THE HEAD AND LINER WERE REPLACED WITHOUT COMPLICATIONS. IT WAS REPORTED THAT NO FURTHER INFORMATION IS AVAILABLE.
Patient problems: Joint Dislocation; Muscle/Tendon Damage
MAUDE report 21332856 ↗InjuryDec 6, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated
NO FURTHER INFORMATION AT THE TIME OF THIS REPORT.
Patient problems: Joint Dislocation; Pain; Scar Tissue
MAUDE report 20863213 ↗InjuryJan 30, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated
IT WAS REPORTED THE PATIENT HAD A LEFT TOTAL HIP ARTHROPLASTY. SIX WEEKS POST-OP, SHE ANTERIORLY DISLOCATED THE HIP WHILE CLIPPING HER TOENAILS AND EXPERIENCED ONGOING PAIN. THE PHYSICIAN NOTED THAT WITH THE DEFORMITY IN THE PATIENT¿S BACK, SHE WOULD BE MORE LIKELY TO DISLOCATE AGAIN. THE PATIENT ANTERIORLY DISLOCATED 3-4 MORE TIMES BEFORE BEING REVISED APPROXIMATELY EIGHT (8) MONTHS AFTER INITIAL SURGERY. DURING THE REVISION, UPON OPENING OF THE CAPSULE, THE HIP WAS FOUND DISLOCATED, THE JOINT HAD THE APPEARANCE OF CHRONIC ANTERIOR HIP DISLOCATION, AND THE POSTERIOR CAPSULAR TISSUES WERE SOMEWHAT TORN. THE TAPER, HEAD, AND LINER WERE EXCHANGED WITHOUT COMPLICATION. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Joint Dislocation; Joint Laxity; Muscle/Tendon Damage; Pain
MAUDE report 16264162 ↗InjuryOct 19, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated
IT WAS REPORTED THAT A PATIENT HAD A LEFT TOTAL HIP ARTHROPLASTY. SUBSEQUENTLY, APPROXIMATELY 3 MONTHS LATER, PATIENT FELT A POP A COUPLE OF TIMES AND MANIPULATIONS WERE PERFORMED TO CORRECT THE DISLOCATIONS. APPROXIMATELY ONE MONTH LATER, PATIENT UNDERWENT A REVISION DUE TO THE RECURRENT DISLOCATIONS. DURING THE REVISION, THE POSTERIOR CAPSULAR STRUCTURES WERE NOTED TO BE TORN OFF THE POSTERIOR GREATER TROCHANTER AND SCARRED DOWN POSTERIORLY OVER THE SCIATIC NERVE. TISSUES WERE DEBRIDED AROUND THE PROXIMAL FEMUR AND DISSECTED AROUND THE PERIMETER OF THE ACETABULAR BASE. LARGE AMOUNTS OF SCAR TISSUE WERE FOUND ANTERIORLY. THE SURGERY WAS COMPLETED WITHOUT COMPLICATION AND THE HEAD, TAPER, AND LINER WERE EXCHANGED WHILE THE ACETABULUM AND STEM WERE FOUND WELL FIXED. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.
Patient problems: Joint Dislocation; Muscle/Tendon Damage; Scar Tissue
MAUDE report 15633027 ↗InjuryApr 18, 2022Device Dislodged or Dislocated; Naturally Worn; Device Dislodged or Dislocated; Naturally Worn
IT WAS REPORTED THE PATIENT UNDERWENT RIGHT INITIAL TOTAL HIP ARTHROPLASTY. SUBSEQUENTLY WAS REVISED APPROXIMATELY 5.5 YEARS LATER DUE TO EXTERNAL TRAUMA CAUSING THE HIP TO DISLOCATE. THE HEAD, NECK, AND LINER WERE EXCHANGED WITHOUT COMPLICATIONS. THE STEM AND CUP REMAINED IMPLANTED. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.
Patient problems: Failure of Implant; Joint Dislocation; Muscle/Tendon Damage
MAUDE report 14137627 ↗InjuryApr 1, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated
IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL HIP ARTHROPLASTY ON AN UNKNOWN DATE. SUBSEQUENTLY, THE PATIENT WAS REVISED DUE TO DISLOCATION. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.
Patient problems: Joint Dislocation
MAUDE report 13977482 ↗InjuryOct 25, 2021Unstable; Device Dislodged or Dislocated; Unstable; Device Dislodged or Dislocated
IT WAS REPORTED THE PATIENT UNDERWENT INITIAL LEFT TOTAL HIP ARTHROPLASTY. SUBSEQUENTLY THE PATIENT WAS REVISED A SECOND TIME DUE TO DISLOCATION AND DISSOCIATED FEMORAL HEAD FROM FALLING OFF STEP APPROXIMATELY 17 YEARS AFTER THE INITIAL THA. DURING THE REVISION A HEMATOMA, SWELLING, SCAR TISSUE, INACCESSIBLE FEMORAL HEAD, AND BONE LOSS WERE NOTED. THE HEAD, CUP, LINER, AND SCREWS WERE EXCHANGED WITHOUT COMPLICATIONS. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.
Patient problems: Fall; Hematoma; Joint Dislocation; Osteopenia/ Osteoporosis; Pain; Swelling/ Edema
MAUDE report 12688889 ↗InjuryOct 30, 2020Unstable; Device Dislodged or Dislocated; Unstable; Device Dislodged or Dislocated
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Joint Dislocation; No Code Available
MAUDE report 10762633 ↗InjuryOct 8, 2020Device Dislodged or Dislocated; Unintended Movement; Device Dislodged or Dislocated; Unintended Movement
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Inflammation; Joint Dislocation; Loss of Range of Motion; Tissue Damage
MAUDE report 10649853 ↗
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 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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