Citation 6265-5116Recalls & reported problems
Howmedica Osteonics Corp. · 132 Degree Neck Angle V40 Hip Stem - Right · Class 2 · Implant
All models of Citation (20)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 07613153074397), received between Mar 29, 2019 and Sep 22, 2025 — classified as 2 injuries, 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (2 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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Detachment of Device or Device Component2
- Degraded1
- Device Dislodged or Dislocated1
- Scratched Material1
Patient problems
- Ambulation or Postural Difficulties1
- Fall1
- Insufficient Information1
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjurySep 22, 2025Degraded; Detachment of Device or Device Component; Degraded; Detachment of Device or Device Component
THE FOLLOWING INFORMATION WAS PROVIDED: CITATION STEM WITH V40 METAL HEAD. WORN TRUNNION CAUSED DISSOCIATION. REVISED WITH 2B STEM AND STRYKER MDM. RIGHT SIDE.
Patient problems: Ambulation or Postural Difficulties; Insufficient Information
MAUDE report 23110359 ↗InjuryAug 3, 2022Detachment of Device or Device Component; Device Dislodged or Dislocated; Detachment of Device or Device Component; Device Dislodged or Dislocated
IT WAS REPORTED THAT THE PATIENT'S LEFT HIP WAS REVISED. PATIENT FELL AND HEAD DISSOCIATION WAS DIAGNOSED (UNKNOWN WHICH ONE CAUSED THE OTHER). INTRA-OPERATIVELY, TRUNNION WEAR WAS NOTED. THE STEM, HEAD, AND LINER WERE REVISED. REP CONFIRMED THERE ARE NO ALLEGATIONS AGAINST THE REVISED LINER. REP CONFIRMED HE WILL PROVIDE ALL PICTURES AND DOCUMENTS AVAILABLE TO HIM FROM THE HOSPITAL AND SURGEON.
Patient problems: Fall
MAUDE report 15154612 ↗MalfunctionMar 29, 2019Scratched Material; Scratched Material
SURGEON IMPLANTED THE FEMORAL STEM INTO THE CANAL AND NOTICED THERE WERE SOME SIGNIFICANT SCRATCHES ON THE TRUNNION. DUE TO THE USE OF THE USE OF A CERAMIC HEAD HE OPTED TO REMOVE THE STEM AND IMPLANT A NEW ONE. SURGEON SAYS THAT IT WAS SCRATCHED OUT OF THE PACKAGE HOWEVER THE STEM WAS IMPLANTED BEFORE THE SCRATCHES WERE NOTICED SO THERE IS NO WAY OF KNOWING.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8466807 ↗
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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