Trident 500-01-50DRecalls & reported problems
Howmedica Osteonics Corp. · Hemispherical Acetabular Shell · Class 2 · Implant
All models of Trident (160)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 07613153072904), received between Mar 15, 2021 and Oct 23, 2023 — classified as 3 injuries.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).
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
- Insufficient Device Problem Information1
- Loss of Osseointegration1
- Malposition of Device1
- Osseointegration Problem1
Patient problems
- Inadequate Osseointegration2
- Pain2
- Metal Related Pathology1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryOct 23, 2023Malposition of Device; Osseointegration Problem; Malposition of Device; Osseointegration Problem
REVISED A LEFT HIP. HE REVISED THE CUP, LINER AND HEAD DUE TO CUP MALPOSITIONING AFTER LOOSENING.
Patient problems: Inadequate Osseointegration
MAUDE report 17983331 ↗InjurySep 22, 2021Loss of Osseointegration; Loss of Osseointegration
RIGHT HIP REVISION FOR PAIN AND ASEPTIC LOOSENING OF THE ACETABULUM. CUP, INSERT, AND HEAD REPLACED. IMPLANTED IN 2004.
Patient problems: Inadequate Osseointegration; Pain
MAUDE report 12511806 ↗InjuryMar 15, 2021Insufficient Device Problem Information; Insufficient Device Problem Information
THIS PI IS FOR REVISION OF PRIMARY. THE PATIENT STATED SHE HAD A RIGHT THA DONE (B)(6) 2007. PATIENT STARTED TO EXPERIENCE PAIN APPROX IN 2011. IN (B)(6) 2020 PATIENT HAD AN MRI AND BLOOD WORK DONE WHICH SHOWED SHE HAD HIGH COBALT LEVELS AND MRI SHOWED LARGE PSEUDOTUMORS. THE PATIENT WAS REVISED ON (B)(6) 2020. AFTER REVISION THE PATIENT EXPERIENCED A LARGE HEMATOMA ON HER RIGHT HIP. THE PATIENT STATED THE HEMATOMA WAS DRAINED THREE TIMES BUT IT KEEPS COMING BACK. THE PATIENT IS SCHEDULED FOR SURGERY ON (B)(6) 2021 TO REMOVE THE HEMATOMA, ANY PRESENT METALS AND PUT A DRAIN FOR ABOUT 5 DAYS. PATIENT IS SEEKING COMPENSATION.
Patient problems: Metal Related Pathology; Pain
MAUDE report 11480259 ↗
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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