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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

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 1 reportsJan 2025: 0 reportsFeb 2025: 1 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 1 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

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

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Sources and updates

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