Trident 502-11-46CRecalls & 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
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04546540432001), received between Oct 26, 2018 and Oct 14, 2019 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Fitting Problem” (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.
Most reported problems
Device problems
- Fitting Problem1
- Positioning Problem1
Patient problems
- Injury1
- Joint Dislocation1
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 14, 2019Fitting Problem; Fitting Problem
THE CUSTOMER REPORTED THAT THE HEMISPHERICAL CLUSTER HOLE SHELL WAS OPENED AND WAS LOOSE IN THE REAMED ACETABULUM, IT APPEARED SMALLER THAN THE REAMER SHELL. **UPDATE** A SIZE 45 REAMER WAS USED (LOT 00153) THE CASE WAS RESOLVED USING A SIZE 46 PSL CUP WITH 2 SCREWS THERE WAS A DELAY OF 10 MINUTES RIGHT SIDE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9186217 ↗InjuryOct 26, 2018Positioning Problem; Positioning Problem
IT WAS REPORTED THAT PATIENT'S RIGHT HIP WAS REVISED DUE TO DISLOCATION. THE ENTIRE CONSTRUCT WAS REVISED (STEM, SHELL, AND METAL LINER WERE REVISED TO ADJUST PATIENT'S VERSION, THERE ARE NO ALLEGATIONS AGAINST THE DEVICES).
Patient problems: Injury; Joint Dislocation
MAUDE report 8010078 ↗
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.
How reports and recalls are matched · Editorial policy · Report an error on this page