Trident 623-00-44HRecalls & reported problems
Howmedica Osteonics Corp. · 0 Degree Polyethylene Insert · Class 2 · Implant
All models of Trident (160)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327025408), received between Jul 2, 2018 and Jan 16, 2020 — classified as 2 injuries.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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 18, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Device Dislodged or Dislocated1
- Insufficient Device Problem Information1
- Mechanical Problem1
Patient problems
- Ambulation or Postural Difficulties1
- Extraskeletal ossification1
- Inadequate Osseointegration1
- Injury1
- Joint Dislocation1
- Osteolysis1
- Pain1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJan 16, 2020Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information; Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information
PATIENT CALLED STATING HE HAD A RIGHT HIP REPLACEMENT DONE ON (B)(6) 2008 AND IS EXPERIENCING PAIN AS HE WALKS. PATIENT ALSO REPORTED THAT HIS DOCTOR MENTIONED BONE LOSS AND LOOSENING IN HIS HIP. PATIENT WOULD LIKE TO KNOW IF HIS IMPLANTS WERE PART OF A RECALL.
Patient problems: Ambulation or Postural Difficulties; Extraskeletal ossification; Inadequate Osseointegration; Osteolysis; Pain
MAUDE report 9597978 ↗InjuryJul 2, 2018Mechanical Problem; Device Dislodged or Dislocated; Mechanical Problem; Device Dislodged or Dislocated
PER MEDICAL REVIEW: WHEN SEEN ON (B)(6) 2016 IT WAS NOTED SHE HAD "DISLOCATED ON (B)(6) 2016 ... EMERGENCY ROOM CLOSED REDUCTION ... X-RAY SLIGHTLY DISPLACED FRACTURE ANTERIOR WALL". ON (B)(6) 2016 THE OFFICE NOTE STATES, "NO FURTHER DISLOCATIONS ... PAIN DOWN POSTERIOR LEG ...
Patient problems: Injury; Joint Dislocation
MAUDE report 7655708 ↗
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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